HGVS | Genome Assembly |
---|---|
NC_000015.10:g.59419496A= , CM000677.2:g.59419496A= | GRCh38 |
NC_000015.9:g.59711695A= , CM000677.1:g.59711695A= | GRCh37 |
NC_000015.8:g.57498987A= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000558348.5:c.-78+17138A= | ENSP00000453918.1:n.-78+17138A= | |
ENST00000560394.5:c.-78+17138A= | ENSP00000452962.1:n.-78+17138A= | |
XM_006720399.1:c.-78+17138A= | XP_006720462.1:n.-78+17138A= | |
XM_011521248.1:c.-22+17138A= | XP_011519550.1:n.-22+17138A= | |
XM_011521248.2:c.-22+17138A= | XP_011519550.1:n.-22+17138A= |