Canonical Allele Identifier: CA357236569

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274366G>T (hg19) ; chr4:g.73408649G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408649G>T , CM000666.2:g.73408649G>T	GRCh38
NC_000004.11:g.74274366G>T , CM000666.1:g.74274366G>T	GRCh37
NC_000004.10:g.74493230G>T	NCBI36
NG_009291.1:g.9395G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.326G>T MANE Select	ENSP00000295897.4:p.Gly109Val
ENST00000295897.8:c.326G>T	ENSP00000295897.4:p.Gly109Val
ENST00000401494.7:c.138-706G>T	ENSP00000384695.3:n.138-706G>T
ENST00000415165.6:c.138-3347G>T	ENSP00000401820.2:n.138-3347G>T
ENST00000441319.5:c.332G>T	ENSP00000392541.1:p.Gly111Val
ENST00000476441.6:c.80-706G>T	ENSP00000423727.1:n.80-706G>T
ENST00000503124.5:c.33-706G>T	ENSP00000421027.1:n.33-706G>T
ENST00000505649.5:n.12G>T
ENST00000509063.5:c.326G>T	ENSP00000422784.1:p.Gly109Val
ENST00000510166.5:n.362G>T
ENST00000514786.1:n.295G>T
ENST00000515133.5:n.367G>T
ENST00000621085.4:c.326G>T	ENSP00000483421.1:p.Gly109Val
ENST00000621628.4:c.326G>T	ENSP00000480485.1:p.Gly109Val
NM_000477.5:c.326G>T	NP_000468.1:p.Gly109Val
NM_000477.6:c.326G>T	NP_000468.1:p.Gly109Val
NM_000477.7:c.326G>T MANE Select	NP_000468.1:p.Gly109Val