Canonical Allele Identifier: CA127937
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18217
ClinVar RCV Id: RCV000019878
dbSNP Id: rs77050410

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406741G>A , CM000666.2:g.73406741G>A GRCh38
NC_000004.11:g.74272458G>A , CM000666.1:g.74272458G>A GRCh37
NC_000004.10:g.74491322G>A NCBI36
NG_009291.1:g.7487G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.250G>A MANE Select ENSP00000295897.4:p.Glu84Lys
ENST00000295897.8:c.250G>A ENSP00000295897.4:p.Glu84Lys
ENST00000401494.7:c.137+1568G>A ENSP00000384695.3:n.137+1568G>A
ENST00000415165.6:c.137+1568G>A ENSP00000401820.2:n.137+1568G>A
ENST00000441319.5:n.256G>A ENSP00000392541.1:p.Glu86Lys
ENST00000476441.6:c.79+2335G>A ENSP00000423727.1:n.79+2335G>A
ENST00000503124.5:c.12G>A ENSP00000421027.1:p.Leu4=
ENST00000509063.5:c.250G>A ENSP00000422784.1:p.Glu84Lys
ENST00000510166.5:n.286G>A
ENST00000514786.1:n.219G>A
ENST00000515133.5:n.291G>A
ENST00000621085.4:c.250G>A ENSP00000483421.1:p.Glu84Lys
ENST00000621628.4:c.250G>A ENSP00000480485.1:p.Glu84Lys
NM_000477.5:c.250G>A NP_000468.1:p.Glu84Lys
NM_000477.6:c.250G>A NP_000468.1:p.Glu84Lys
NM_000477.7:c.250G>A MANE Select NP_000468.1:p.Glu84Lys