Linked Data
dbSNP Id:
rs11264799
gnomAD v2:
1-157670757-C-T
gnomAD v3:
1-157700967-C-T
gnomAD v4:
1-157700967-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.157700967C>T , CM000663.2:g.157700967C>T | GRCh38 |
| NC_000001.10:g.157670757C>T , CM000663.1:g.157670757C>T | GRCh37 |
| NC_000001.9:g.155937381C>T | NCBI36 |
| NG_023241.1:g.4891G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_006711145.1:c.-204G>A | XP_006711208.1:n.-204G>A |