HGVS | Genome Assembly |
---|---|
NC_000015.10:g.44711347C>A , CM000677.2:g.44711347C>A | GRCh38 |
NC_000015.9:g.45003545C>A , CM000677.1:g.45003545C>A | GRCh37 |
NC_000015.8:g.42790837C>A | NCBI36 |
NG_012920.1:g.4861C>A | |
NG_012920.2:g.4871C>A |
HGVS | Amino-acid Change | |
---|---|---|
XM_011521338.1:c.-581G>T | XP_011519640.1:n.-581G>T | |
XM_011521339.1:c.-462G>T | XP_011519641.1:n.-462G>T | |
XM_011521340.1:c.-403G>T | XP_011519642.1:n.-403G>T | |
XM_011521343.1:c.-665G>T | XP_011519645.1:n.-665G>T | |
XM_011521345.1:c.-636G>T | XP_011519647.1:n.-636G>T | |
XM_011521338.3:c.-581G>T | XP_011519640.1:n.-581G>T | |
XM_011521339.3:c.-462G>T | XP_011519641.1:n.-462G>T | |
XM_011521340.3:c.-403G>T | XP_011519642.1:n.-403G>T | |
XM_011521343.3:c.-665G>T | XP_011519645.1:n.-665G>T | |
XM_011521345.3:c.-636G>T | XP_011519647.1:n.-636G>T | |
NM_001387260.1:c.-91G>T | NP_001374189.1:n.-91G>T |