Linked Data
ClinVar Variation Id:
1667785
ClinVar RCV Id:
RCV002189245
dbSNP Id:
rs1833370518
gnomAD v4:
9-137158713-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137158713C>T , CM000671.2:g.137158713C>T | GRCh38 |
| NC_000009.11:g.140053165C>T , CM000671.1:g.140053165C>T | GRCh37 |
| NC_000009.10:g.139172986C>T | NCBI36 |
| NG_011507.1:g.24557C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371553.8:c.1260+9C>T | ENSP00000360608.3:n.1260+9C>T | |
| ENST00000371560.5:c.1260+9C>T | ENSP00000360615.3:n.1260+9C>T | |
| ENST00000371561.8:c.1197+9C>T MANE Select | ENSP00000360616.3:n.1197+9C>T | |
| ENST00000675295.1:n.627+9C>T | ||
| ENST00000676396.1:n.2716C>T | ||
| ENST00000350902.9:c.*172+9C>T | ENSP00000316915.9:n.*172+9C>T | |
| ENST00000371546.8:c.1260+9C>T | ENSP00000360601.4:n.1260+9C>T | |
| ENST00000371550.8:c.1197+9C>T | ENSP00000360605.4:n.1197+9C>T | |
| ENST00000371553.7:c.1260+9C>T | ENSP00000360608.3:n.1260+9C>T | |
| ENST00000371555.8:c.1260+9C>T | ENSP00000360610.4:n.1260+9C>T | |
| ENST00000371559.8:c.1197+9C>T | ENSP00000360614.4:n.1197+9C>T | |
| ENST00000371560.4:c.1260+9C>T | ENSP00000360615.3:n.1260+9C>T | |
| ENST00000371561.7:c.1197+9C>T | ENSP00000360616.3:n.1197+9C>T | |
| ENST00000471122.5:n.1274+9C>T | ||
| ENST00000485413.1:n.397C>T | ||
| NM_000832.6:c.1197+9C>T | NP_000823.4:n.1197+9C>T | |
| NM_001185090.1:c.1260+9C>T | NP_001172019.1:n.1260+9C>T | |
| NM_001185091.1:c.1260+9C>T | NP_001172020.1:n.1260+9C>T | |
| NM_007327.3:c.1197+9C>T | NP_015566.1:n.1197+9C>T | |
| NM_021569.3:c.1197+9C>T | NP_067544.1:n.1197+9C>T | |
| XM_005266071.2:c.1197+9C>T | XP_005266128.1:n.1197+9C>T | |
| XM_005266072.2:c.1260+9C>T | XP_005266129.1:n.1260+9C>T | |
| XM_005266073.3:c.1260+9C>T | XP_005266130.1:n.1260+9C>T | |
| XM_011518583.1:c.1260+9C>T | XP_011516885.1:n.1260+9C>T | |
| XM_005266071.3:c.1197+9C>T | XP_005266128.1:n.1197+9C>T | |
| XM_005266072.3:c.1260+9C>T | XP_005266129.1:n.1260+9C>T | |
| XM_005266073.4:c.1260+9C>T | XP_005266130.1:n.1260+9C>T | |
| XM_011518583.2:c.1260+9C>T | XP_011516885.1:n.1260+9C>T | |
| NM_007327.4:c.1197+9C>T MANE Select | NP_015566.1:n.1197+9C>T | |
| NM_000832.7:c.1197+9C>T | NP_000823.4:n.1197+9C>T | |
| NM_001185090.2:c.1260+9C>T | NP_001172019.1:n.1260+9C>T | |
| NM_001185091.2:c.1260+9C>T | NP_001172020.1:n.1260+9C>T | |
| NM_021569.4:c.1197+9C>T | NP_067544.1:n.1197+9C>T |