Linked Data
ClinVar Variation Id:
101328
ClinVar RCV Id:
RCV000087566
dbSNP Id:
rs587779610
gnomAD v4:
2-189007528-G-A
COSMIC:
COSM137826
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189007528G>A , CM000664.2:g.189007528G>A | GRCh38 |
| NC_000002.11:g.189872254G>A , CM000664.1:g.189872254G>A | GRCh37 |
| NC_000002.10:g.189580499G>A | NCBI36 |
| NG_007404.1:g.38156G>A , LRG_3:g.38156G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.3185G>A | ENSP00000415346.2:p.Gly1062Asp | |
| ENST00000304636.9:c.3284G>A MANE Select | ENSP00000304408.4:p.Gly1095Asp | |
| ENST00000304636.7:c.3284G>A | ENSP00000304408.3:p.Gly1095Asp | |
| ENST00000317840.9:c.2528-526G>A | ENSP00000315243.6:n.2528-526G>A | |
| NM_000090.3:c.3284G>A , LRG_3t1:c.3284G>A | NP_000081.1:p.Gly1095Asp | |
| NM_000090.4:c.3284G>A MANE Select | NP_000081.2:p.Gly1095Asp |