Canonical Allele Identifier: CA357244416

Gene: ALB

Linked Data

• dbSNP Id: rs2149329535
• MyVariant Identifiers: chr4:g.74283875G>A (hg19) ; chr4:g.73418158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418158G>A , CM000666.2:g.73418158G>A	GRCh38
NC_000004.11:g.74283875G>A , CM000666.1:g.74283875G>A	GRCh37
NC_000004.10:g.74502739G>A	NCBI36
NG_009291.1:g.18904G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1499G>A MANE Select	ENSP00000295897.4:p.Cys500Tyr
ENST00000295897.8:c.1499G>A	ENSP00000295897.4:p.Cys500Tyr
ENST00000401494.7:c.1154G>A	ENSP00000384695.3:p.Cys385Tyr
ENST00000415165.6:c.923G>A	ENSP00000401820.2:p.Cys308Tyr
ENST00000476441.6:c.*778G>A	ENSP00000423727.1:n.*778G>A
ENST00000486939.1:n.153G>A
ENST00000503124.5:c.1049G>A	ENSP00000421027.1:p.Cys350Tyr
ENST00000505649.5:n.1046G>A
ENST00000509063.5:c.1499G>A	ENSP00000422784.1:p.Cys500Tyr
ENST00000511370.1:c.1032G>A
ENST00000621085.4:c.860G>A	ENSP00000483421.1:p.Cys287Tyr
ENST00000621628.4:c.860G>A	ENSP00000480485.1:p.Cys287Tyr
NM_000477.5:c.1499G>A	NP_000468.1:p.Cys500Tyr
NM_000477.6:c.1499G>A	NP_000468.1:p.Cys500Tyr
NM_000477.7:c.1499G>A MANE Select	NP_000468.1:p.Cys500Tyr