Linked Data
dbSNP Id:
rs1008315409
gnomAD v2:
20-3649078-C-A
gnomAD v3:
20-3668431-C-A
gnomAD v4:
20-3668431-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3668431C>A , CM000682.2:g.3668431C>A | GRCh38 |
| NC_000020.10:g.3649078C>A , CM000682.1:g.3649078C>A | GRCh37 |
| NC_000020.9:g.3597078C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000356518.7:c.*532G>T MANE Select | ENSP00000348912.3:n.*532G>T | |
| ENST00000350009.6:c.*532G>T | ENSP00000322550.5:n.*532G>T | |
| ENST00000356518.6:c.*532G>T | ENSP00000348912.2:n.*532G>T | |
| ENST00000379861.8:c.*532G>T | ENSP00000369190.4:n.*532G>T | |
| ENST00000466620.5:n.2535G>T | ||
| ENST00000483362.1:n.1897G>T | ||
| ENST00000619289.4:c.*532G>T | ENSP00000484600.1:n.*532G>T | |
| NM_001282447.1:c.*532G>T | NP_001269376.1:n.*532G>T | |
| NM_025220.3:c.*532G>T | NP_079496.1:n.*532G>T | |
| NM_153202.2:c.*532G>T | NP_694882.1:n.*532G>T | |
| XM_005260843.1:c.*532G>T | XP_005260900.1:n.*532G>T | |
| XM_006723639.1:c.*532G>T | XP_006723702.1:n.*532G>T | |
| XM_006723640.1:c.*532G>T | XP_006723703.1:n.*532G>T | |
| XM_011529366.1:c.*532G>T | XP_011527668.1:n.*532G>T | |
| XM_011529367.1:c.*532G>T | XP_011527669.1:n.*532G>T | |
| XM_011529368.1:c.*532G>T | XP_011527670.1:n.*532G>T | |
| XM_011529373.1:c.*532G>T | XP_011527675.1:n.*532G>T | |
| XR_937153.1:n.2995G>T | ||
| XR_937154.1:n.2995G>T | ||
| XR_937155.1:n.2916G>T | ||
| XR_937157.1:n.2918G>T | ||
| NM_001282447.2:c.*532G>T | NP_001269376.1:n.*532G>T | |
| NM_025220.4:c.*532G>T | NP_079496.1:n.*532G>T | |
| NM_153202.3:c.*532G>T | NP_694882.1:n.*532G>T | |
| XM_011529373.2:c.*532G>T | XP_011527675.1:n.*532G>T | |
| XR_001754405.1:n.3082G>T | ||
| XR_002958534.1:n.3191G>T | ||
| NM_001282447.3:c.*532G>T | NP_001269376.1:n.*532G>T | |
| NM_025220.5:c.*532G>T MANE Select | NP_079496.1:n.*532G>T | |
| NM_153202.4:c.*532G>T | NP_694882.1:n.*532G>T |