HGVS | Genome Assembly |
---|---|
NC_000013.11:g.28659104G>A , CM000675.2:g.28659104G>A | GRCh38 |
NC_000013.10:g.29233241G>A , CM000675.1:g.29233241G>A | GRCh37 |
NC_000013.9:g.28131241G>A | NCBI36 |
NG_027550.1:g.5101G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000697716.1:c.-166G>A | ENSP00000513414.1:n.-166G>A | |
ENST00000380842.4:c.-81G>A | ENSP00000370222.4:n.-81G>A | |
ENST00000460403.1:n.1G>A | ||
NM_015932.5:c.-81G>A | NP_057016.1:n.-81G>A |