HGVS | Genome Assembly |
---|---|
NC_000002.12:g.38076402G>A , CM000664.2:g.38076402G>A | GRCh38 |
NC_000002.11:g.38303544G>A , CM000664.1:g.38303544G>A | GRCh37 |
NC_000002.10:g.38157048G>A | NCBI36 |
NG_008386.2:g.4700C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000494864.1:c.-70-5092C>T | ENSP00000479876.1:n.-70-5092C>T | |
XM_011533236.1:c.1016G>A | XP_011531538.1:p.Cys339Tyr |