Canonical Allele Identifier: CA357238065

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74275092G>T (hg19) ; chr4:g.73409375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409375G>T , CM000666.2:g.73409375G>T	GRCh38
NC_000004.11:g.74275092G>T , CM000666.1:g.74275092G>T	GRCh37
NC_000004.10:g.74493956G>T	NCBI36
NG_009291.1:g.10121G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.503G>T MANE Select	ENSP00000295897.4:p.Arg168Ile
ENST00000295897.8:c.503G>T	ENSP00000295897.4:p.Arg168Ile
ENST00000401494.7:c.158G>T	ENSP00000384695.3:p.Arg53Ile
ENST00000415165.6:c.138-2621G>T	ENSP00000401820.2:n.138-2621G>T
ENST00000441319.5:c.509G>T	ENSP00000392541.1:p.Arg170Ile
ENST00000476441.6:c.100G>T	ENSP00000423727.1:p.Glu34Ter
ENST00000503124.5:c.53G>T	ENSP00000421027.1:p.Arg18Ile
ENST00000505649.5:n.189G>T
ENST00000509063.5:c.503G>T	ENSP00000422784.1:p.Arg168Ile
ENST00000511370.1:c.36G>T
ENST00000514786.1:n.472G>T
ENST00000621085.4:c.490+13G>T	ENSP00000483421.1:n.490+13G>T
ENST00000621628.4:c.486+299G>T	ENSP00000480485.1:n.486+299G>T
NM_000477.5:c.503G>T	NP_000468.1:p.Arg168Ile
NM_000477.6:c.503G>T	NP_000468.1:p.Arg168Ile
NM_000477.7:c.503G>T MANE Select	NP_000468.1:p.Arg168Ile