HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12720601G>T , CM000686.2:g.12720601G>T | GRCh38 |
NC_000024.9:g.14832534G>T , CM000686.1:g.14832534G>T | GRCh37 |
NC_000024.8:g.13341928G>T | NCBI36 |
NG_008311.1:g.24375G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651177.1:c.109G>T | ENSP00000498372.1:p.Asp37Tyr | |
ENST00000338981.7:c.109G>T MANE Select | ENSP00000342812.3:p.Asp37Tyr | |
ENST00000426564.6:n.121G>T | ||
ENST00000493168.1:n.185G>T | ||
NM_004654.3:c.109G>T | NP_004645.2:p.Asp37Tyr | |
XM_011531469.1:c.109G>T | XP_011529771.1:p.Asp37Tyr | |
XM_011531470.1:c.-126G>T | XP_011529772.1:n.-126G>T | |
XM_017030078.2:c.109G>T | XP_016885567.1:p.Asp37Tyr | |
NM_004654.4:c.109G>T MANE Select | NP_004645.2:p.Asp37Tyr |