Canonical Allele Identifier: CA99711694

Gene: ALB

Linked Data

• dbSNP Id: rs532514465
• gnomAD v3: 4-73419465-G-A
• gnomAD v4: 4-73419465-G-A
• MyVariant Identifiers: chr4:g.74285182G>A (hg19) ; chr4:g.73419465G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419465G>A , CM000666.2:g.73419465G>A	GRCh38
NC_000004.11:g.74285182G>A , CM000666.1:g.74285182G>A	GRCh37
NC_000004.10:g.74504046G>A	NCBI36
NG_009291.1:g.20211G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1653-42G>A MANE Select	ENSP00000295897.4:n.1653-42G>A
ENST00000295897.8:c.1653-42G>A	ENSP00000295897.4:n.1653-42G>A
ENST00000401494.7:c.1308-42G>A	ENSP00000384695.3:n.1308-42G>A
ENST00000415165.6:c.1077-42G>A	ENSP00000401820.2:n.1077-42G>A
ENST00000476441.6:c.*932-42G>A	ENSP00000423727.1:n.*932-42G>A
ENST00000486939.1:n.307-42G>A
ENST00000503124.5:c.1203-42G>A	ENSP00000421027.1:n.1203-42G>A
ENST00000505649.5:n.1200-42G>A
ENST00000508932.5:n.175+10G>A
ENST00000509063.5:c.1653-42G>A	ENSP00000422784.1:n.1653-42G>A
ENST00000511370.1:c.1186-42G>A
ENST00000621085.4:c.1014-42G>A	ENSP00000483421.1:n.1014-42G>A
ENST00000621628.4:c.1014-42G>A	ENSP00000480485.1:n.1014-42G>A
NM_000477.5:c.1653-42G>A	NP_000468.1:n.1653-42G>A
NM_000477.6:c.1653-42G>A	NP_000468.1:n.1653-42G>A
NM_000477.7:c.1653-42G>A MANE Select	NP_000468.1:n.1653-42G>A