Canonical Allele Identifier: CA439800877

Gene: ALB

Linked Data

• ClinVar Variation Id: 905525
• ClinVar RCV Id: RCV001154096
• dbSNP Id: rs57636959
• gnomAD v2: 4-74285251-G-A
• gnomAD v3: 4-73419534-G-A
• gnomAD v4: 4-73419534-G-A
• MyVariant Identifiers: chr4:g.74285251G>A (hg19) ; chr4:g.73419534G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419534G>A , CM000666.2:g.73419534G>A	GRCh38
NC_000004.11:g.74285251G>A , CM000666.1:g.74285251G>A	GRCh37
NC_000004.10:g.74504115G>A	NCBI36
NG_009291.1:g.20280G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1680G>A MANE Select	ENSP00000295897.4:p.Lys560=
ENST00000295897.8:c.1680G>A	ENSP00000295897.4:p.Lys560=
ENST00000401494.7:c.1335G>A	ENSP00000384695.3:p.Lys445=
ENST00000415165.6:c.1104G>A	ENSP00000401820.2:p.Lys368=
ENST00000476441.6:c.*959G>A	ENSP00000423727.1:n.*959G>A
ENST00000486939.1:n.334G>A
ENST00000503124.5:c.1230G>A	ENSP00000421027.1:p.Lys410=
ENST00000505649.5:n.1227G>A
ENST00000508932.5:n.175+79G>A
ENST00000509063.5:c.1680G>A	ENSP00000422784.1:p.Lys560=
ENST00000511370.1:c.1213G>A
ENST00000621085.4:c.1041G>A	ENSP00000483421.1:p.Lys347=
ENST00000621628.4:c.1041G>A	ENSP00000480485.1:p.Lys347=
NM_000477.5:c.1680G>A	NP_000468.1:p.Lys560=
NM_000477.6:c.1680G>A	NP_000468.1:p.Lys560=
NM_000477.7:c.1680G>A MANE Select	NP_000468.1:p.Lys560=