HGVS | Genome Assembly |
---|---|
NC_000015.10:g.40405756G>T , CM000677.2:g.40405756G>T | GRCh38 |
NC_000015.9:g.40697957G>T , CM000677.1:g.40697957G>T | GRCh37 |
NC_000015.8:g.38485249G>T | NCBI36 |
NG_011986.1:g.5272G>T | |
NG_011986.2:g.5272G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650656.1:c.-63G>T | ENSP00000498731.1:n.-63G>T | |
ENST00000651168.1:c.-63G>T | ENSP00000499074.1:n.-63G>T | |
NM_001159508.1:c.-63G>T | NP_001152980.1:n.-63G>T | |
NM_002225.3:c.-63G>T | NP_002216.2:n.-63G>T | |
XR_429453.2:n.39G>T |