Canonical Allele Identifier: CA552307098

Gene: ALB

Linked Data

• dbSNP Id: rs1357864329
• gnomAD v2: 4-74285197-T-A
• gnomAD v4: 4-73419480-T-A
• MyVariant Identifiers: chr4:g.74285197T>A (hg19) ; chr4:g.73419480T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419480T>A , CM000666.2:g.73419480T>A	GRCh38
NC_000004.11:g.74285197T>A , CM000666.1:g.74285197T>A	GRCh37
NC_000004.10:g.74504061T>A	NCBI36
NG_009291.1:g.20226T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1653-27T>A MANE Select	ENSP00000295897.4:n.1653-27T>A
ENST00000295897.8:c.1653-27T>A	ENSP00000295897.4:n.1653-27T>A
ENST00000401494.7:c.1308-27T>A	ENSP00000384695.3:n.1308-27T>A
ENST00000415165.6:c.1077-27T>A	ENSP00000401820.2:n.1077-27T>A
ENST00000476441.6:c.*932-27T>A	ENSP00000423727.1:n.*932-27T>A
ENST00000486939.1:n.307-27T>A
ENST00000503124.5:c.1203-27T>A	ENSP00000421027.1:n.1203-27T>A
ENST00000505649.5:n.1200-27T>A
ENST00000508932.5:n.175+25T>A
ENST00000509063.5:c.1653-27T>A	ENSP00000422784.1:n.1653-27T>A
ENST00000511370.1:c.1186-27T>A
ENST00000621085.4:c.1014-27T>A	ENSP00000483421.1:n.1014-27T>A
ENST00000621628.4:c.1014-27T>A	ENSP00000480485.1:n.1014-27T>A
NM_000477.5:c.1653-27T>A	NP_000468.1:n.1653-27T>A
NM_000477.6:c.1653-27T>A	NP_000468.1:n.1653-27T>A
NM_000477.7:c.1653-27T>A MANE Select	NP_000468.1:n.1653-27T>A