HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12857655T>G , CM000686.2:g.12857655T>G | GRCh38 |
NC_000024.9:g.14969580T>G , CM000686.1:g.14969580T>G | GRCh37 |
NC_000024.8:g.13478974T>G | NCBI36 |
NG_008311.1:g.161421T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651177.1:c.7524T>G | ENSP00000498372.1:p.Tyr2508Ter | |
ENST00000338981.7:c.7524T>G MANE Select | ENSP00000342812.3:p.Tyr2508Ter | |
ENST00000426564.6:n.7551T>G | ||
ENST00000453031.1:c.569T>G | ||
ENST00000471409.1:n.843T>G | ||
NM_004654.3:c.7524T>G | NP_004645.2:p.Tyr2508Ter | |
XM_011531469.1:c.7524T>G | XP_011529771.1:p.Tyr2508Ter | |
XM_011531470.1:c.7290T>G | XP_011529772.1:p.Tyr2430Ter | |
XM_017030078.2:c.7539T>G | XP_016885567.1:p.Tyr2513Ter | |
NM_004654.4:c.7524T>G MANE Select | NP_004645.2:p.Tyr2508Ter |