HGVS | Genome Assembly |
---|---|
NC_000005.10:g.96399005C>T , CM000667.2:g.96399005C>T | GRCh38 |
NC_000005.9:g.95734709C>T , CM000667.1:g.95734709C>T | GRCh37 |
NC_000005.8:g.95760465C>T | NCBI36 |
NG_021161.1:g.39277G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000311106.8:c.1462G>A MANE Select | ENSP00000308024.2:p.Glu488Lys | |
ENST00000311106.7:c.1462G>A | ENSP00000308024.2:p.Glu488Lys | |
ENST00000508626.5:c.1321G>A | ENSP00000421600.1:p.Glu441Lys | |
ENST00000513085.1:n.605G>A | ||
NM_000439.4:c.1462G>A | NP_000430.3:p.Glu488Lys | |
NM_001177875.1:c.1321G>A | NP_001171346.1:p.Glu441Lys | |
NR_130776.1:n.354+19353C>T | ||
NM_000439.5:c.1462G>A MANE Select | NP_000430.3:p.Glu488Lys | |
NM_001177875.2:c.1321G>A | NP_001171346.1:p.Glu441Lys |