Linked Data
ClinVar Variation Id:
2991922
ClinVar RCV Id:
RCV003852985
dbSNP Id:
rs771116175
gnomAD v2:
2-128183791-C-T
gnomAD v3:
2-127426215-C-T
gnomAD v4:
2-127426215-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.127426215C>T , CM000664.2:g.127426215C>T | GRCh38 |
| NC_000002.11:g.128183791C>T , CM000664.1:g.128183791C>T | GRCh37 |
| NC_000002.10:g.127900261C>T | NCBI36 |
| NG_016323.1:g.12796C>T , LRG_599:g.12796C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000234071.8:c.666C>T MANE Select | ENSP00000234071.4:p.Asp222= | |
| ENST00000234071.7:c.666C>T | ENSP00000234071.3:p.Asp222= | |
| ENST00000402125.2:c.121-2142C>T | ||
| ENST00000409048.1:c.768C>T | ENSP00000386679.1:p.Asp256= | |
| ENST00000464089.1:n.252C>T | ||
| NM_000312.3:c.666C>T , LRG_599t1:c.666C>T | NP_000303.1:p.Asp222= | |
| XM_005263715.3:c.849C>T | XP_005263772.1:p.Asp283= | |
| XM_005263716.3:c.831C>T | XP_005263773.1:p.Asp277= | |
| XM_005263717.3:c.729C>T | XP_005263774.1:p.Asp243= | |
| XM_005263717.4:c.729C>T | XP_005263774.1:p.Asp243= | |
| XM_017004505.1:c.909C>T | XP_016859994.1:p.Asp303= | |
| XM_024453002.1:c.1011C>T | XP_024308770.1:p.Asp337= | |
| XM_024453003.1:c.951C>T | XP_024308771.1:p.Asp317= | |
| XM_024453004.1:c.849C>T | XP_024308772.1:p.Asp283= | |
| XM_024453005.1:c.831C>T | XP_024308773.1:p.Asp277= | |
| XM_024453006.1:c.768C>T | XP_024308774.1:p.Asp256= | |
| XR_923313.2:n.4370G>A | ||
| NM_000312.4:c.666C>T MANE Select | NP_000303.1:p.Asp222= | |
| NM_001375602.1:c.849C>T | NP_001362531.1:p.Asp283= | |
| NM_001375603.1:c.831C>T | NP_001362532.1:p.Asp277= | |
| NM_001375604.1:c.729C>T | NP_001362533.1:p.Asp243= | |
| NM_001375605.1:c.768C>T | NP_001362534.1:p.Asp256= | |
| NM_001375606.1:c.834C>T | NP_001362535.1:p.Asp278= | |
| NM_001375607.1:c.852C>T | NP_001362536.1:p.Asp284= | |
| NM_001375608.1:c.609C>T | NP_001362537.1:p.Asp203= | |
| NM_001375609.1:c.642C>T | NP_001362538.1:p.Asp214= | |
| NM_001375610.1:c.660C>T | NP_001362539.1:p.Asp220= | |
| NM_001375611.1:c.666C>T | NP_001362540.1:p.Asp222= | |
| NM_001375613.1:c.666C>T | NP_001362542.1:p.Asp222= |