Canonical Allele Identifier: CA357235796

Gene: ALB

Linked Data

• dbSNP Id: rs1577934980
• gnomAD v4: 4-73406717-A-G
• MyVariant Identifiers: chr4:g.74272434A>G (hg19) ; chr4:g.73406717A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406717A>G , CM000666.2:g.73406717A>G	GRCh38
NC_000004.11:g.74272434A>G , CM000666.1:g.74272434A>G	GRCh37
NC_000004.10:g.74491298A>G	NCBI36
NG_009291.1:g.7463A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.226A>G MANE Select	ENSP00000295897.4:p.Thr76Ala
ENST00000295897.8:c.226A>G	ENSP00000295897.4:p.Thr76Ala
ENST00000401494.7:c.137+1544A>G	ENSP00000384695.3:n.137+1544A>G
ENST00000415165.6:c.137+1544A>G	ENSP00000401820.2:n.137+1544A>G
ENST00000441319.5:c.232A>G	ENSP00000392541.1:p.Thr78Ala
ENST00000476441.6:c.79+2311A>G	ENSP00000423727.1:n.79+2311A>G
ENST00000503124.5:c.-13A>G	ENSP00000421027.1:n.-13A>G
ENST00000509063.5:c.226A>G	ENSP00000422784.1:p.Thr76Ala
ENST00000510166.5:n.262A>G
ENST00000514786.1:n.195A>G
ENST00000515133.5:n.267A>G
ENST00000621085.4:c.226A>G	ENSP00000483421.1:p.Thr76Ala
ENST00000621628.4:c.226A>G	ENSP00000480485.1:p.Thr76Ala
NM_000477.5:c.226A>G	NP_000468.1:p.Thr76Ala
NM_000477.6:c.226A>G	NP_000468.1:p.Thr76Ala
NM_000477.7:c.226A>G MANE Select	NP_000468.1:p.Thr76Ala