HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927968T>A , CM000663.2:g.149927968T>A | GRCh38 |
NC_000001.10:g.149899860T>A , CM000663.1:g.149899860T>A | GRCh37 |
NC_000001.9:g.148166484T>A | NCBI36 |
NG_032777.1:g.5285A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-209A>T | ENSP00000271628.8:n.-209A>T | |
NM_005850.4:c.-209A>T | NP_005841.1:n.-209A>T |