Linked Data
dbSNP Id:
rs1322767371
gnomAD v2:
8-55540415-G-A
gnomAD v4:
8-54627855-G-A
COSMIC:
COSM1472106
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.54627855G>A , CM000670.2:g.54627855G>A | GRCh38 |
| NC_000008.10:g.55540415G>A , CM000670.1:g.55540415G>A | GRCh37 |
| NC_000008.9:g.55702968G>A | NCBI36 |
| NG_009840.1:g.16789G>A | |
| NG_009840.2:g.16789G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220676.2:c.3973G>A MANE Select | ENSP00000220676.1:p.Gly1325Arg | |
| ENST00000636932.1:c.787+5567G>A | ENSP00000489857.1:n.787+5567G>A | |
| ENST00000637698.1:c.787+5567G>A | ENSP00000490104.1:n.787+5567G>A | |
| ENST00000220676.1:c.3973G>A | ENSP00000220676.1:p.Gly1325Arg | |
| NM_006269.1:c.3973G>A | NP_006260.1:p.Gly1325Arg | |
| XM_017013721.1:c.3994G>A | XP_016869210.1:p.Gly1332Arg | |
| XM_017013722.1:c.3973G>A | XP_016869211.1:p.Gly1325Arg | |
| NM_001375654.1:c.787+5567G>A | NP_001362583.1:n.787+5567G>A | |
| NM_006269.2:c.3973G>A MANE Select | NP_006260.1:p.Gly1325Arg |