Canonical Allele Identifier: CA357246288

Gene: ALB

Linked Data

• dbSNP Id: rs1383190524
• gnomAD v3: 4-73419565-G-A
• gnomAD v4: 4-73419565-G-A
• MyVariant Identifiers: chr4:g.74285282G>A (hg19) ; chr4:g.73419565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419565G>A , CM000666.2:g.73419565G>A	GRCh38
NC_000004.11:g.74285282G>A , CM000666.1:g.74285282G>A	GRCh37
NC_000004.10:g.74504146G>A	NCBI36
NG_009291.1:g.20311G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1711G>A MANE Select	ENSP00000295897.4:p.Val571Ile
ENST00000295897.8:c.1711G>A	ENSP00000295897.4:p.Val571Ile
ENST00000401494.7:c.1366G>A	ENSP00000384695.3:p.Val456Ile
ENST00000415165.6:c.1135G>A	ENSP00000401820.2:p.Val379Ile
ENST00000476441.6:c.*990G>A	ENSP00000423727.1:n.*990G>A
ENST00000495173.1:n.19G>A
ENST00000503124.5:c.1261G>A	ENSP00000421027.1:p.Val421Ile
ENST00000505649.5:n.1258G>A
ENST00000508932.5:n.175+110G>A
ENST00000509063.5:c.1711G>A	ENSP00000422784.1:p.Val571Ile
ENST00000511370.1:c.1244G>A
ENST00000621085.4:c.1072G>A	ENSP00000483421.1:p.Val358Ile
ENST00000621628.4:c.1072G>A	ENSP00000480485.1:p.Val358Ile
NM_000477.5:c.1711G>A	NP_000468.1:p.Val571Ile
NM_000477.6:c.1711G>A	NP_000468.1:p.Val571Ile
NM_000477.7:c.1711G>A MANE Select	NP_000468.1:p.Val571Ile