HGVS | Genome Assembly |
---|---|
NC_000002.12:g.170813570A>T , CM000664.2:g.170813570A>T | GRCh38 |
NC_000002.11:g.171670080A>T , CM000664.1:g.171670080A>T | GRCh37 |
NC_000002.10:g.171378326A>T | NCBI36 |
NG_021477.1:g.1881A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000454603.5:c.-64+148A>T | ENSP00000402366.1:n.-64+148A>T | |
XM_011510922.1:c.-64+148A>T | XP_011509224.1:n.-64+148A>T |