Canonical Allele Identifier: CA439948402

Gene: ALB

Linked Data

• dbSNP Id: rs1577941858
• MyVariant Identifiers: chr4:g.74283951G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418234G>A , CM000666.2:g.73418234G>A	GRCh38
NC_000004.11:g.74283951G>A , CM000666.1:g.74283951G>A	GRCh37
NC_000004.10:g.74502815G>A	NCBI36
NG_009291.1:g.18980G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1575G>A MANE Select	ENSP00000295897.4:p.Glu525=
ENST00000295897.8:c.1575G>A	ENSP00000295897.4:p.Glu525=
ENST00000401494.7:c.1230G>A	ENSP00000384695.3:p.Glu410=
ENST00000415165.6:c.999G>A	ENSP00000401820.2:p.Glu333=
ENST00000476441.6:c.*854G>A	ENSP00000423727.1:n.*854G>A
ENST00000486939.1:n.229G>A
ENST00000503124.5:c.1125G>A	ENSP00000421027.1:p.Glu375=
ENST00000505649.5:n.1122G>A
ENST00000509063.5:c.1575G>A	ENSP00000422784.1:p.Glu525=
ENST00000511370.1:c.1108G>A
ENST00000621085.4:c.936G>A	ENSP00000483421.1:p.Glu312=
ENST00000621628.4:c.936G>A	ENSP00000480485.1:p.Glu312=
NM_000477.5:c.1575G>A	NP_000468.1:p.Glu525=
NM_000477.6:c.1575G>A	NP_000468.1:p.Glu525=
NM_000477.7:c.1575G>A MANE Select	NP_000468.1:p.Glu525=