Canonical Allele Identifier: CA357246236

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285272A>T (hg19) ; chr4:g.73419555A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419555A>T , CM000666.2:g.73419555A>T	GRCh38
NC_000004.11:g.74285272A>T , CM000666.1:g.74285272A>T	GRCh37
NC_000004.10:g.74504136A>T	NCBI36
NG_009291.1:g.20301A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1701A>T MANE Select	ENSP00000295897.4:p.Gln567His
ENST00000295897.8:c.1701A>T	ENSP00000295897.4:p.Gln567His
ENST00000401494.7:c.1356A>T	ENSP00000384695.3:p.Gln452His
ENST00000415165.6:c.1125A>T	ENSP00000401820.2:p.Gln375His
ENST00000476441.6:c.*980A>T	ENSP00000423727.1:n.*980A>T
ENST00000495173.1:n.9A>T
ENST00000503124.5:c.1251A>T	ENSP00000421027.1:p.Gln417His
ENST00000505649.5:n.1248A>T
ENST00000508932.5:n.175+100A>T
ENST00000509063.5:c.1701A>T	ENSP00000422784.1:p.Gln567His
ENST00000511370.1:c.1234A>T
ENST00000621085.4:c.1062A>T	ENSP00000483421.1:p.Gln354His
ENST00000621628.4:c.1062A>T	ENSP00000480485.1:p.Gln354His
NM_000477.5:c.1701A>T	NP_000468.1:p.Gln567His
NM_000477.6:c.1701A>T	NP_000468.1:p.Gln567His
NM_000477.7:c.1701A>T MANE Select	NP_000468.1:p.Gln567His