HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27323130T>A , CM000664.2:g.27323130T>A | GRCh38 |
NC_000002.11:g.27545997T>A , CM000664.1:g.27545997T>A | GRCh37 |
NC_000002.10:g.27399501T>A | NCBI36 |
NG_008075.1:g.4435A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357186.10:c.18+1303A>T | ENSP00000349713.6:n.18+1303A>T | |
XM_005264327.2:c.-208A>T | XP_005264384.1:n.-208A>T |