Linked Data
ClinVar Variation Id:
2661
dbSNP Id:
rs587777811
gnomAD v3:
7-33177592-G-C
gnomAD v4:
7-33177592-G-C
PubMed:
PMID:16380913
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.33177592G>C , CM000669.2:g.33177592G>C | GRCh38 |
| NC_000007.13:g.33217204G>C , CM000669.1:g.33217204G>C | GRCh37 |
| NC_000007.12:g.33183729G>C | NCBI36 |
| NG_009306.1:g.53053G>C | |
| NG_009306.2:g.53349G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242067.11:c.442+1G>C MANE Select | ENSP00000242067.6:n.442+1G>C | |
| ENST00000671871.1:c.565+1G>C | ENSP00000499908.1:n.565+1G>C | |
| ENST00000671890.1:c.307+1G>C | ENSP00000500146.1:n.307+1G>C | |
| ENST00000671952.1:c.442+1G>C | ENSP00000500239.1:n.442+1G>C | |
| ENST00000671963.1:c.76+1G>C | ENSP00000499904.1:n.76+1G>C | |
| ENST00000672453.1:n.211+1G>C | ||
| ENST00000672717.1:c.442+1G>C | ENSP00000499835.1:n.442+1G>C | |
| ENST00000672973.1:c.442+1G>C | ENSP00000500017.1:n.442+1G>C | |
| ENST00000673056.1:c.442+1G>C | ENSP00000499989.1:n.442+1G>C | |
| ENST00000673219.1:c.*179+1G>C | ENSP00000499968.1:n.*179+1G>C | |
| ENST00000673230.1:n.473+1G>C | ||
| ENST00000673431.1:c.307+1G>C | ENSP00000500552.1:n.307+1G>C | |
| ENST00000673462.1:c.442+1G>C | ENSP00000499848.1:n.442+1G>C | |
| ENST00000242067.10:c.442+1G>C | ENSP00000242067.6:n.442+1G>C | |
| ENST00000350941.7:c.442+1G>C | ENSP00000313122.6:n.442+1G>C | |
| ENST00000355070.6:c.442+1G>C | ENSP00000347182.2:n.442+1G>C | |
| ENST00000396127.6:c.442+1G>C | ENSP00000379433.2:n.442+1G>C | |
| ENST00000425508.6:c.307+1G>C | ENSP00000405151.2:n.307+1G>C | |
| ENST00000433714.5:c.442+1G>C | ENSP00000412159.1:n.442+1G>C | |
| ENST00000442858.1:c.76+1G>C | ENSP00000388646.1:n.76+1G>C | |
| NM_001033604.1:c.442+1G>C | NP_001028776.1:n.442+1G>C | |
| NM_001033605.1:c.442+1G>C | NP_001028777.1:n.442+1G>C | |
| NM_014451.3:c.442+1G>C | NP_055266.2:n.442+1G>C | |
| NM_198428.2:c.442+1G>C | NP_940820.1:n.442+1G>C | |
| XM_005249700.3:c.442+1G>C | XP_005249757.1:n.442+1G>C | |
| XM_005249701.1:c.442+1G>C | XP_005249758.1:n.442+1G>C | |
| XM_011515264.1:c.442+1G>C | XP_011513566.1:n.442+1G>C | |
| XM_011515265.1:c.442+1G>C | XP_011513567.1:n.442+1G>C | |
| XM_011515266.1:c.442+1G>C | XP_011513568.1:n.442+1G>C | |
| XM_011515267.1:c.442+1G>C | XP_011513569.1:n.442+1G>C | |
| XM_011515268.1:c.442+1G>C | XP_011513570.1:n.442+1G>C | |
| XM_011515269.1:c.169+1G>C | XP_011513571.1:n.169+1G>C | |
| XM_011515270.1:c.442+1G>C | XP_011513572.1:n.442+1G>C | |
| NM_001348036.1:c.442+1G>C | NP_001334965.1:n.442+1G>C | |
| NM_001348037.2:c.76+1G>C | NP_001334966.1:n.76+1G>C | |
| NM_001348038.2:c.169+1G>C | NP_001334967.1:n.169+1G>C | |
| NM_001348039.2:c.169+1G>C | NP_001334968.1:n.169+1G>C | |
| NM_001348040.2:c.442+1G>C | NP_001334969.1:n.442+1G>C | |
| NM_001348041.3:c.442+1G>C | NP_001334970.1:n.442+1G>C | |
| NM_001348042.2:c.307+1G>C | NP_001334971.1:n.307+1G>C | |
| NM_001348043.2:c.442+1G>C | NP_001334972.1:n.442+1G>C | |
| NM_001348044.2:c.76+1G>C | NP_001334973.1:n.76+1G>C | |
| NM_001348045.2:c.76+1G>C | NP_001334974.1:n.76+1G>C | |
| NM_001348046.2:c.76+1G>C | NP_001334975.1:n.76+1G>C | |
| NM_001362679.1:c.442+1G>C | NP_001349608.1:n.442+1G>C | |
| NR_145411.1:n.721+1G>C | ||
| NR_145412.1:n.721+1G>C | ||
| NR_145413.2:n.955+1G>C | ||
| XM_005249701.3:c.442+1G>C | XP_005249758.1:n.442+1G>C | |
| XM_011515265.2:c.442+1G>C | XP_011513567.1:n.442+1G>C | |
| XM_011515266.3:c.442+1G>C | XP_011513568.1:n.442+1G>C | |
| XM_011515267.3:c.442+1G>C | XP_011513569.1:n.442+1G>C | |
| XM_011515269.2:c.169+1G>C | XP_011513571.1:n.169+1G>C | |
| XM_011515270.3:c.442+1G>C | XP_011513572.1:n.442+1G>C | |
| XM_017011990.1:c.442+1G>C | XP_016867479.1:n.442+1G>C | |
| XM_017011994.2:c.442+1G>C | XP_016867483.1:n.442+1G>C | |
| XR_001744634.2:n.945+1G>C | ||
| NM_001348040.3:c.442+1G>C | NP_001334969.1:n.442+1G>C | |
| NM_001348041.4:c.442+1G>C | NP_001334970.1:n.442+1G>C | |
| NM_001348043.3:c.442+1G>C | NP_001334972.1:n.442+1G>C | |
| NM_198428.3:c.442+1G>C MANE Select | NP_940820.1:n.442+1G>C | |
| NM_001033604.2:c.442+1G>C | NP_001028776.1:n.442+1G>C | |
| NM_001033605.2:c.442+1G>C | NP_001028777.1:n.442+1G>C | |
| NM_001348037.3:c.76+1G>C | NP_001334966.1:n.76+1G>C | |
| NM_001348038.3:c.169+1G>C | NP_001334967.1:n.169+1G>C | |
| NM_001348039.3:c.169+1G>C | NP_001334968.1:n.169+1G>C | |
| NM_001348042.3:c.307+1G>C | NP_001334971.1:n.307+1G>C | |
| NM_001348044.3:c.76+1G>C | NP_001334973.1:n.76+1G>C | |
| NM_001348045.3:c.76+1G>C | NP_001334974.1:n.76+1G>C | |
| NM_001348046.3:c.76+1G>C | NP_001334975.1:n.76+1G>C | |
| NM_014451.4:c.442+1G>C | NP_055266.2:n.442+1G>C | |
| NR_145413.3:n.931+1G>C |