Canonical Allele Identifier: CA439800872

Gene: ALB

Linked Data

• dbSNP Id: rs1381201686
• gnomAD v2: 4-74285242-G-A
• gnomAD v4: 4-73419525-G-A
• MyVariant Identifiers: chr4:g.74285242G>A (hg19) ; chr4:g.73419525G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419525G>A , CM000666.2:g.73419525G>A	GRCh38
NC_000004.11:g.74285242G>A , CM000666.1:g.74285242G>A	GRCh37
NC_000004.10:g.74504106G>A	NCBI36
NG_009291.1:g.20271G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1671G>A MANE Select	ENSP00000295897.4:p.Val557=
ENST00000295897.8:c.1671G>A	ENSP00000295897.4:p.Val557=
ENST00000401494.7:c.1326G>A	ENSP00000384695.3:p.Val442=
ENST00000415165.6:c.1095G>A	ENSP00000401820.2:p.Val365=
ENST00000476441.6:c.*950G>A	ENSP00000423727.1:n.*950G>A
ENST00000486939.1:n.325G>A
ENST00000503124.5:c.1221G>A	ENSP00000421027.1:p.Val407=
ENST00000505649.5:n.1218G>A
ENST00000508932.5:n.175+70G>A
ENST00000509063.5:c.1671G>A	ENSP00000422784.1:p.Val557=
ENST00000511370.1:c.1204G>A
ENST00000621085.4:c.1032G>A	ENSP00000483421.1:p.Val344=
ENST00000621628.4:c.1032G>A	ENSP00000480485.1:p.Val344=
NM_000477.5:c.1671G>A	NP_000468.1:p.Val557=
NM_000477.6:c.1671G>A	NP_000468.1:p.Val557=
NM_000477.7:c.1671G>A MANE Select	NP_000468.1:p.Val557=