HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48472609T>A , CM000677.2:g.48472609T>A | GRCh38 |
NC_000015.9:g.48764806T>A , CM000677.1:g.48764806T>A | GRCh37 |
NC_000015.8:g.46552098T>A | NCBI36 |
NG_008805.2:g.178180A>T , LRG_778:g.178180A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4278A>T | ENSP00000453958.2:p.Gly1426= | |
ENST00000674301.2:c.4278A>T | ENSP00000501333.2:p.Gly1426= | |
ENST00000683268.1:n.245A>T | ||
ENST00000684448.1:n.2952A>T | ||
ENST00000316623.10:c.4278A>T MANE Select | ENSP00000325527.5:p.Gly1426= | |
ENST00000316623.9:c.4278A>T | ENSP00000325527.5:p.Gly1426= | |
ENST00000537463.6:c.*41A>T | ENSP00000440294.2:n.*41A>T | |
NM_000138.4:c.4278A>T , LRG_778t1:c.4278A>T | NP_000129.3:p.Gly1426= | |
NM_000138.5:c.4278A>T MANE Select | NP_000129.3:p.Gly1426= |