HGVS | Genome Assembly |
---|---|
NC_000001.11:g.179575953T>A , CM000663.2:g.179575953T>A | GRCh38 |
NC_000001.10:g.179545088T>A , CM000663.1:g.179545088T>A | GRCh37 |
NC_000001.9:g.177811711T>A | NCBI36 |
NG_007535.1:g.4997A>T , LRG_887:g.4997A>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_005245483.2:c.-89A>T | XP_005245540.1:n.-89A>T | |
XM_006711529.2:c.-89A>T | XP_006711592.1:n.-89A>T | |
XM_005245483.3:c.-89A>T | XP_005245540.1:n.-89A>T | |
XM_017002298.1:c.-89A>T | XP_016857787.1:n.-89A>T | |
XM_017002299.1:c.-89A>T | XP_016857788.1:n.-89A>T |