HGVS | Genome Assembly |
---|---|
NC_000001.11:g.62447362A>G , CM000663.2:g.62447362A>G | GRCh38 |
NC_000001.10:g.62913033A>G , CM000663.1:g.62913033A>G | GRCh37 |
NC_000001.9:g.62685621A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000339950.5:c.1271A>G MANE Select | ENSP00000343526.4:p.Glu424Gly | |
ENST00000339950.4:c.1271A>G | ENSP00000343526.4:p.Glu424Gly | |
ENST00000371146.5:c.1271A>G | ENSP00000360188.1:p.Glu424Gly | |
NM_001017415.1:c.1271A>G | NP_001017415.1:p.Glu424Gly | |
NM_001017416.1:c.1271A>G | NP_001017416.1:p.Glu424Gly | |
NM_003368.4:c.1271A>G | NP_003359.3:p.Glu424Gly | |
NM_003368.5:c.1271A>G MANE Select | NP_003359.3:p.Glu424Gly | |
NM_001017415.2:c.1271A>G | NP_001017415.1:p.Glu424Gly | |
NM_001017416.2:c.1271A>G | NP_001017416.1:p.Glu424Gly |