Canonical Allele Identifier: CA357240562

Gene: ALB

Linked Data

• dbSNP Id: rs1222078466
• gnomAD v3: 4-73413465-A-G
• gnomAD v4: 4-73413465-A-G
• MyVariant Identifiers: chr4:g.74279182A>G (hg19) ; chr4:g.73413465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413465A>G , CM000666.2:g.73413465A>G	GRCh38
NC_000004.11:g.74279182A>G , CM000666.1:g.74279182A>G	GRCh37
NC_000004.10:g.74498046A>G	NCBI36
NG_009291.1:g.14211A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.889A>G MANE Select	ENSP00000295897.4:p.Ser297Gly
ENST00000295897.8:c.889A>G	ENSP00000295897.4:p.Ser297Gly
ENST00000401494.7:c.544A>G	ENSP00000384695.3:p.Ser182Gly
ENST00000415165.6:c.313A>G	ENSP00000401820.2:p.Ser105Gly
ENST00000476441.6:c.*168A>G	ENSP00000423727.1:n.*168A>G
ENST00000484992.1:n.209A>G
ENST00000503124.5:c.439A>G	ENSP00000421027.1:p.Ser147Gly
ENST00000505649.5:n.575A>G
ENST00000509063.5:c.889A>G	ENSP00000422784.1:p.Ser297Gly
ENST00000511370.1:c.422A>G
ENST00000621085.4:c.491-1641A>G	ENSP00000483421.1:n.491-1641A>G
ENST00000621628.4:c.487-1637A>G	ENSP00000480485.1:n.487-1637A>G
NM_000477.5:c.889A>G	NP_000468.1:p.Ser297Gly
NM_000477.6:c.889A>G	NP_000468.1:p.Ser297Gly
NM_000477.7:c.889A>G MANE Select	NP_000468.1:p.Ser297Gly