HGVS | Genome Assembly |
---|---|
NC_000001.11:g.241847971T>C , CM000663.2:g.241847971T>C | GRCh38 |
NC_000001.10:g.242011273T>C , CM000663.1:g.242011273T>C | GRCh37 |
NC_000001.9:g.240077896T>C | NCBI36 |
NG_029100.1:g.4781T>C | |
NG_029100.2:g.4781T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000519225.5:c.-544T>C | ENSP00000429720.1:n.-544T>C | |
XM_011544322.1:c.-544T>C | XP_011542624.1:n.-544T>C |