Canonical Allele Identifier: CA357244776

Gene: ALB

Linked Data

• dbSNP Id: rs1560860000
• gnomAD v3: 4-73418218-C-A
• gnomAD v4: 4-73418218-C-A
• MyVariant Identifiers: chr4:g.74283935C>A (hg19) ; chr4:g.73418218C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418218C>A , CM000666.2:g.73418218C>A	GRCh38
NC_000004.11:g.74283935C>A , CM000666.1:g.74283935C>A	GRCh37
NC_000004.10:g.74502799C>A	NCBI36
NG_009291.1:g.18964C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1559C>A MANE Select	ENSP00000295897.4:p.Thr520Lys
ENST00000295897.8:c.1559C>A	ENSP00000295897.4:p.Thr520Lys
ENST00000401494.7:c.1214C>A	ENSP00000384695.3:p.Thr405Lys
ENST00000415165.6:c.983C>A	ENSP00000401820.2:p.Thr328Lys
ENST00000476441.6:c.*838C>A	ENSP00000423727.1:n.*838C>A
ENST00000486939.1:n.213C>A
ENST00000503124.5:c.1109C>A	ENSP00000421027.1:p.Thr370Lys
ENST00000505649.5:n.1106C>A
ENST00000509063.5:c.1559C>A	ENSP00000422784.1:p.Thr520Lys
ENST00000511370.1:c.1092C>A
ENST00000621085.4:c.920C>A	ENSP00000483421.1:p.Thr307Lys
ENST00000621628.4:c.920C>A	ENSP00000480485.1:p.Thr307Lys
NM_000477.5:c.1559C>A	NP_000468.1:p.Thr520Lys
NM_000477.6:c.1559C>A	NP_000468.1:p.Thr520Lys
NM_000477.7:c.1559C>A MANE Select	NP_000468.1:p.Thr520Lys