HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12833699A>G , CM000686.2:g.12833699A>G | GRCh38 |
NC_000024.9:g.14945625A>G , CM000686.1:g.14945625A>G | GRCh37 |
NC_000024.8:g.13455019A>G | NCBI36 |
NG_008311.1:g.137466A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651177.1:c.5033A>G | ENSP00000498372.1:p.Glu1678Gly | |
ENST00000338981.7:c.5033A>G MANE Select | ENSP00000342812.3:p.Glu1678Gly | |
ENST00000426564.6:n.5045A>G | ||
NM_004654.3:c.5033A>G | NP_004645.2:p.Glu1678Gly | |
XM_011531469.1:c.5033A>G | XP_011529771.1:p.Glu1678Gly | |
XM_011531470.1:c.4799A>G | XP_011529772.1:p.Glu1600Gly | |
XM_017030078.2:c.5048A>G | XP_016885567.1:p.Glu1683Gly | |
NM_004654.4:c.5033A>G MANE Select | NP_004645.2:p.Glu1678Gly |