Linked Data
dbSNP Id:
rs780027455
gnomAD v2:
21-45753052-C-G
gnomAD v3:
21-44333169-C-G
gnomAD v4:
21-44333169-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44333169C>G , CM000683.2:g.44333169C>G | GRCh38 |
| NC_000021.8:g.45753052C>G , CM000683.1:g.45753052C>G | GRCh37 |
| NC_000021.7:g.44577480C>G | NCBI36 |
| NG_032952.1:g.11234G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000339818.9:c.237G>C MANE Select | ENSP00000344566.4:p.Glu79Asp | |
| ENST00000325223.7:c.237G>C | ENSP00000317302.7:p.Glu79Asp | |
| ENST00000339818.8:c.237G>C | ENSP00000344566.4:p.Glu79Asp | |
| ENST00000397956.7:c.237G>C | ENSP00000381047.3:p.Glu79Asp | |
| ENST00000462742.1:n.2408G>C | ||
| ENST00000478674.1:n.296G>C | ||
| ENST00000496321.5:n.353G>C | ||
| NM_001271440.1:c.237G>C | NP_001258369.1:p.Glu79Asp | |
| NM_001271441.1:c.237G>C | NP_001258370.1:p.Glu79Asp | |
| NM_001271442.1:c.114G>C | NP_001258371.1:p.Glu38Asp | |
| NM_004928.2:c.237G>C | NP_004919.1:p.Glu79Asp | |
| XM_006724051.2:c.312G>C | XP_006724114.1:p.Glu104Asp | |
| XM_006724052.2:c.312G>C | XP_006724115.1:p.Glu104Asp | |
| XM_006724053.2:c.-88G>C | XP_006724116.1:n.-88G>C | |
| XR_937571.1:n.440G>C | ||
| XM_006724051.3:c.312G>C | XP_006724114.1:p.Glu104Asp | |
| XM_006724053.3:c.-88G>C | XP_006724116.1:n.-88G>C | |
| XM_017028470.1:c.441G>C | XP_016883959.1:p.Glu147Asp | |
| XM_017028471.1:c.186G>C | XP_016883960.1:p.Glu62Asp | |
| XM_017028472.1:c.-88G>C | XP_016883961.1:n.-88G>C | |
| XR_937571.2:n.447G>C | ||
| NM_004928.3:c.237G>C MANE Select | NP_004919.1:p.Glu79Asp | |
| NM_001271440.2:c.237G>C | NP_001258369.1:p.Glu79Asp | |
| NM_001271441.2:c.237G>C | NP_001258370.1:p.Glu79Asp |