Linked Data
ClinVar Variation Id:
1598048
ClinVar RCV Id:
RCV002120176
dbSNP Id:
rs1832560651
gnomAD v3:
7-103635529-G-A
gnomAD v4:
7-103635529-G-A
COSMIC:
COSM3631614
MyVariant Identifiers:
chr7:g.103275976G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.103635529G>A , CM000669.2:g.103635529G>A | GRCh38 |
| NC_000007.13:g.103275976G>A , CM000669.1:g.103275976G>A | GRCh37 |
| NC_000007.12:g.103063212G>A | NCBI36 |
| NG_011877.1:g.358988C>T | |
| NG_011877.2:g.358988C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000424685.3:c.2361C>T | ENSP00000388446.3:p.Ala787= | |
| ENST00000428762.6:c.2361C>T MANE Select | ENSP00000392423.1:p.Ala787= | |
| ENST00000473457.2:n.2625C>T | ||
| ENST00000679867.1:n.2245C>T | ||
| ENST00000680706.1:n.64C>T | ||
| ENST00000680712.1:n.2078C>T | ||
| ENST00000681034.1:c.2361C>T | ENSP00000506075.1:p.Ala787= | |
| ENST00000343529.9:c.2361C>T | ENSP00000345694.5:p.Ala787= | |
| ENST00000424685.2:c.2361C>T | ENSP00000388446.2:p.Ala787= | |
| ENST00000428762.5:c.2361C>T | ENSP00000392423.1:p.Ala787= | |
| NM_005045.3:c.2361C>T | NP_005036.2:p.Ala787= | |
| NM_173054.2:c.2361C>T | NP_774959.1:p.Ala787= | |
| NM_005045.4:c.2361C>T MANE Select | NP_005036.2:p.Ala787= | |
| NM_173054.3:c.2361C>T | NP_774959.1:p.Ala787= |