Linked Data
dbSNP Id:
rs779307630
gnomAD v2:
17-7979132-C-T
gnomAD v3:
17-8075814-C-T
gnomAD v4:
17-8075814-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8075814C>T , CM000679.2:g.8075814C>T | GRCh38 |
| NC_000017.10:g.7979132C>T , CM000679.1:g.7979132C>T | GRCh37 |
| NC_000017.9:g.7919857C>T | NCBI36 |
| NG_007099.1:g.16890G>A | |
| NG_007099.2:g.16903G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647874.1:c.1533-98G>A MANE Select | ENSP00000497784.1:n.1533-98G>A | |
| ENST00000649809.1:c.597-98G>A | ENSP00000496845.1:n.597-98G>A | |
| ENST00000319144.4:c.1533-98G>A | ENSP00000315167.4:n.1533-98G>A | |
| ENST00000577351.5:n.479+361G>A | ||
| NM_001139.2:c.1533-98G>A | NP_001130.1:n.1533-98G>A | |
| NM_001139.3:c.1533-98G>A MANE Select | NP_001130.1:n.1533-98G>A |