Canonical Allele Identifier: CA357246722

Gene: ALB

Linked Data

• dbSNP Id: rs1719098402
• MyVariant Identifiers: chr4:g.74285348G>A (hg19) ; chr4:g.73419631G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419631G>A , CM000666.2:g.73419631G>A	GRCh38
NC_000004.11:g.74285348G>A , CM000666.1:g.74285348G>A	GRCh37
NC_000004.10:g.74504212G>A	NCBI36
NG_009291.1:g.20377G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1777G>A MANE Select	ENSP00000295897.4:p.Ala593Thr
ENST00000295897.8:c.1777G>A	ENSP00000295897.4:p.Ala593Thr
ENST00000401494.7:c.1432G>A	ENSP00000384695.3:p.Ala478Thr
ENST00000415165.6:c.1201G>A	ENSP00000401820.2:p.Ala401Thr
ENST00000476441.6:c.*1056G>A	ENSP00000423727.1:n.*1056G>A
ENST00000495173.1:n.85G>A
ENST00000503124.5:c.1327G>A	ENSP00000421027.1:p.Ala443Thr
ENST00000505649.5:n.1324G>A
ENST00000508932.5:n.175+176G>A
ENST00000509063.5:c.1777G>A	ENSP00000422784.1:p.Ala593Thr
ENST00000511370.1:c.1310G>A
ENST00000621085.4:c.1138G>A	ENSP00000483421.1:p.Ala380Thr
ENST00000621628.4:c.1138G>A	ENSP00000480485.1:p.Ala380Thr
NM_000477.5:c.1777G>A	NP_000468.1:p.Ala593Thr
NM_000477.6:c.1777G>A	NP_000468.1:p.Ala593Thr
NM_000477.7:c.1777G>A MANE Select	NP_000468.1:p.Ala593Thr