Canonical Allele Identifier: CA127894

Gene: ALB

Linked Data

• dbSNP Id: rs78953271
• MyVariant Identifiers: chr4:g.74279323G>A (hg19) ; chr4:g.73413606G>A (hg38)
• PubMed: PMID:2339130

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413606G>A , CM000666.2:g.73413606G>A	GRCh38
NC_000004.11:g.74279323G>A , CM000666.1:g.74279323G>A	GRCh37
NC_000004.10:g.74498187G>A	NCBI36
NG_009291.1:g.14352G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1030G>A MANE Select	ENSP00000295897.4:p.Ala344Thr
ENST00000295897.8:c.1030G>A	ENSP00000295897.4:p.Ala344Thr
ENST00000401494.7:c.685G>A	ENSP00000384695.3:p.Ala229Thr
ENST00000415165.6:c.454G>A	ENSP00000401820.2:p.Ala152Thr
ENST00000476441.6:c.*309G>A	ENSP00000423727.1:n.*309G>A
ENST00000484992.1:n.350G>A
ENST00000503124.5:c.580G>A	ENSP00000421027.1:p.Ala194Thr
ENST00000504043.1:n.33G>A
ENST00000505649.5:n.716G>A
ENST00000509063.5:c.1030G>A	ENSP00000422784.1:p.Ala344Thr
ENST00000511370.1:c.563G>A
ENST00000621085.4:c.491-1500G>A	ENSP00000483421.1:n.491-1500G>A
ENST00000621628.4:c.487-1496G>A	ENSP00000480485.1:n.487-1496G>A
NM_000477.5:c.1030G>A	NP_000468.1:p.Ala344Thr
NM_000477.6:c.1030G>A	NP_000468.1:p.Ala344Thr
NM_000477.7:c.1030G>A MANE Select	NP_000468.1:p.Ala344Thr