Linked Data
dbSNP Id:
rs1319107811
gnomAD v2:
3-48602896-C-T
gnomAD v4:
3-48565463-C-T
COSMIC:
COSM1045847
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48565463C>T , CM000665.2:g.48565463C>T | GRCh38 |
| NC_000003.11:g.48602896C>T , CM000665.1:g.48602896C>T | GRCh37 |
| NC_000003.10:g.48577900C>T | NCBI36 |
| NG_007065.1:g.34790G>A , LRG_286:g.34790G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681320.1:c.8474G>A MANE Select | ENSP00000506558.1:p.Gly2825Asp | |
| ENST00000328333.12:c.8474G>A | ENSP00000332371.8:p.Gly2825Asp | |
| ENST00000487017.5:n.5113G>A | ||
| NM_000094.3:c.8474G>A , LRG_286t1:c.8474G>A | NP_000085.1:p.Gly2825Asp | |
| XM_011533336.1:c.8501G>A | XP_011531638.1:p.Gly2834Asp | |
| XM_011533337.1:c.8474G>A | XP_011531639.1:p.Gly2825Asp | |
| XM_011533338.1:c.8441G>A | XP_011531640.1:p.Gly2814Asp | |
| XR_940369.1:n.8537G>A | ||
| XR_940370.1:n.8537G>A | ||
| XR_940371.1:n.8537G>A | ||
| XM_017005688.1:c.8414G>A | XP_016861177.1:p.Gly2805Asp | |
| XR_001740003.1:n.8510G>A | ||
| XR_001740004.1:n.8510G>A | ||
| XR_001740005.1:n.8510G>A | ||
| NM_000094.4:c.8474G>A MANE Select | NP_000085.1:p.Gly2825Asp |