Canonical Allele Identifier: CA439798715

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74272391A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406674A>G , CM000666.2:g.73406674A>G	GRCh38
NC_000004.11:g.74272391A>G , CM000666.1:g.74272391A>G	GRCh37
NC_000004.10:g.74491255A>G	NCBI36
NG_009291.1:g.7420A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.183A>G MANE Select	ENSP00000295897.4:p.Glu61=
ENST00000295897.8:c.183A>G	ENSP00000295897.4:p.Glu61=
ENST00000401494.7:c.137+1501A>G	ENSP00000384695.3:n.137+1501A>G
ENST00000415165.6:c.137+1501A>G	ENSP00000401820.2:n.137+1501A>G
ENST00000441319.5:c.189A>G	ENSP00000392541.1:p.Glu63=
ENST00000476441.6:c.79+2268A>G	ENSP00000423727.1:n.79+2268A>G
ENST00000503124.5:c.-56A>G	ENSP00000421027.1:n.-56A>G
ENST00000509063.5:c.183A>G	ENSP00000422784.1:p.Glu61=
ENST00000510166.5:n.219A>G
ENST00000514786.1:n.152A>G
ENST00000515133.5:n.224A>G
ENST00000621085.4:c.183A>G	ENSP00000483421.1:p.Glu61=
ENST00000621628.4:c.183A>G	ENSP00000480485.1:p.Glu61=
NM_000477.5:c.183A>G	NP_000468.1:p.Glu61=
NM_000477.6:c.183A>G	NP_000468.1:p.Glu61=
NM_000477.7:c.183A>G MANE Select	NP_000468.1:p.Glu61=