Linked Data
dbSNP Id:
rs1275267079
gnomAD v2:
2-98355674-C-A
gnomAD v3:
2-97739211-C-A
gnomAD v4:
2-97739211-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.97739211C>A , CM000664.2:g.97739211C>A | GRCh38 |
| NC_000002.11:g.98355674C>A , CM000664.1:g.98355674C>A | GRCh37 |
| NC_000002.10:g.97722106C>A | NCBI36 |
| NG_007727.1:g.30644C>A , LRG_126:g.30644C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698508.1:c.1737-164C>A | ENSP00000513759.1:n.1737-164C>A | |
| ENST00000698509.1:n.1877-164C>A | ||
| ENST00000264972.10:c.1737-164C>A MANE Select | ENSP00000264972.5:n.1737-164C>A | |
| ENST00000264972.9:c.1737-164C>A | ENSP00000264972.5:n.1737-164C>A | |
| ENST00000451498.2:c.816-164C>A | ENSP00000400475.2:n.816-164C>A | |
| ENST00000463643.5:n.1598-164C>A | ||
| ENST00000487283.5:n.2789-164C>A | ||
| NM_001079.3:c.1737-164C>A , LRG_126t1:c.1737-164C>A | NP_001070.2:n.1737-164C>A | |
| NM_207519.1:c.816-164C>A | NP_997402.1:n.816-164C>A | |
| XM_005264015.3:c.1719-164C>A | XP_005264072.1:n.1719-164C>A | |
| XM_011511783.1:c.1736+1104C>A | XP_011510085.1:n.1736+1104C>A | |
| XR_923018.1:n.1938+1104C>A | ||
| XR_923019.1:n.1938+1104C>A | ||
| XR_923020.1:n.2148-164C>A | ||
| XM_017004867.1:c.2106-164C>A | XP_016860356.1:n.2106-164C>A | |
| XM_017004868.1:c.2088-164C>A | XP_016860357.1:n.2088-164C>A | |
| XM_017004869.1:c.2105+1104C>A | XP_016860358.1:n.2105+1104C>A | |
| XR_001738925.1:n.3344+1104C>A | ||
| XR_001738926.1:n.3344+1104C>A | ||
| XR_001738927.1:n.3554-164C>A | ||
| NM_001079.4:c.1737-164C>A MANE Select | NP_001070.2:n.1737-164C>A | |
| NM_001378594.1:c.1737-164C>A | NP_001365523.1:n.1737-164C>A | |
| NM_207519.2:c.816-164C>A | NP_997402.1:n.816-164C>A |