HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12736019G>T , CM000686.2:g.12736019G>T | GRCh38 |
NC_000024.9:g.14847953G>T , CM000686.1:g.14847953G>T | GRCh37 |
NC_000024.8:g.13357347G>T | NCBI36 |
NG_008311.1:g.39794G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651177.1:c.795G>T | ENSP00000498372.1:p.Glu265Asp | |
ENST00000338981.7:c.795G>T MANE Select | ENSP00000342812.3:p.Glu265Asp | |
ENST00000426564.6:n.807G>T | ||
NM_004654.3:c.795G>T | NP_004645.2:p.Glu265Asp | |
XM_011531469.1:c.795G>T | XP_011529771.1:p.Glu265Asp | |
XM_011531470.1:c.561G>T | XP_011529772.1:p.Glu187Asp | |
XM_017030078.2:c.795G>T | XP_016885567.1:p.Glu265Asp | |
NM_004654.4:c.795G>T MANE Select | NP_004645.2:p.Glu265Asp |