Canonical Allele Identifier: CA439948114

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279169A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413452A>G , CM000666.2:g.73413452A>G	GRCh38
NC_000004.11:g.74279169A>G , CM000666.1:g.74279169A>G	GRCh37
NC_000004.10:g.74498033A>G	NCBI36
NG_009291.1:g.14198A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.876A>G MANE Select	ENSP00000295897.4:p.Gln292=
ENST00000295897.8:c.876A>G	ENSP00000295897.4:p.Gln292=
ENST00000401494.7:c.531A>G	ENSP00000384695.3:p.Gln177=
ENST00000415165.6:c.300A>G	ENSP00000401820.2:p.Gln100=
ENST00000476441.6:c.*155A>G	ENSP00000423727.1:n.*155A>G
ENST00000484992.1:n.196A>G
ENST00000503124.5:c.426A>G	ENSP00000421027.1:p.Gln142=
ENST00000505649.5:n.562A>G
ENST00000509063.5:c.876A>G	ENSP00000422784.1:p.Gln292=
ENST00000511370.1:c.409A>G
ENST00000621085.4:c.491-1654A>G	ENSP00000483421.1:n.491-1654A>G
ENST00000621628.4:c.487-1650A>G	ENSP00000480485.1:n.487-1650A>G
NM_000477.5:c.876A>G	NP_000468.1:p.Gln292=
NM_000477.6:c.876A>G	NP_000468.1:p.Gln292=
NM_000477.7:c.876A>G MANE Select	NP_000468.1:p.Gln292=