dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.99161494C>T , CM000669.2:g.99161494C>T | GRCh38 |
| NC_000007.13:g.98759117C>T , CM000669.1:g.98759117C>T | GRCh37 |
| NC_000007.12:g.98597053C>T | NCBI36 |
| NG_051213.1:g.62924G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017012211.1:c.1546-15178G>A | XP_016867700.1:n.1546-15178G>A |