HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20760003G>T , CM000686.2:g.20760003G>T | GRCh38 |
NC_000024.9:g.22921889G>T , CM000686.1:g.22921889G>T | GRCh37 |
NC_000024.8:g.21331277G>T | NCBI36 |
NG_032924.1:g.8936G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000629237.2:c.217G>T MANE Select | ENSP00000486252.1:p.Asp73Tyr | |
ENST00000629237.1:c.217G>T | ENSP00000486252.1:p.Asp73Tyr | |
NM_001039567.2:c.217G>T | NP_001034656.1:p.Asp73Tyr | |
XM_011531423.1:c.166G>T | XP_011529725.1:p.Asp56Tyr | |
NM_001039567.3:c.217G>T MANE Select | NP_001034656.1:p.Asp73Tyr |