Canonical Allele Identifier: CA99705409

Gene: ALB

Linked Data

• dbSNP Id: rs901613471
• gnomAD v2: 4-74279074-G-A
• gnomAD v3: 4-73413357-G-A
• gnomAD v4: 4-73413357-G-A
• MyVariant Identifiers: chr4:g.74279074G>A (hg19) ; chr4:g.73413357G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413357G>A , CM000666.2:g.73413357G>A	GRCh38
NC_000004.11:g.74279074G>A , CM000666.1:g.74279074G>A	GRCh37
NC_000004.10:g.74497938G>A	NCBI36
NG_009291.1:g.14103G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-63G>A MANE Select	ENSP00000295897.4:n.844-63G>A
ENST00000295897.8:c.844-63G>A	ENSP00000295897.4:n.844-63G>A
ENST00000401494.7:c.499-63G>A	ENSP00000384695.3:n.499-63G>A
ENST00000415165.6:c.268-63G>A	ENSP00000401820.2:n.268-63G>A
ENST00000476441.6:c.*123-63G>A	ENSP00000423727.1:n.*123-63G>A
ENST00000484992.1:n.101G>A
ENST00000503124.5:c.394-63G>A	ENSP00000421027.1:n.394-63G>A
ENST00000505649.5:n.530-63G>A
ENST00000509063.5:c.844-63G>A	ENSP00000422784.1:n.844-63G>A
ENST00000511370.1:c.377-63G>A
ENST00000621085.4:c.491-1749G>A	ENSP00000483421.1:n.491-1749G>A
ENST00000621628.4:c.487-1745G>A	ENSP00000480485.1:n.487-1745G>A
NM_000477.5:c.844-63G>A	NP_000468.1:n.844-63G>A
NM_000477.6:c.844-63G>A	NP_000468.1:n.844-63G>A
NM_000477.7:c.844-63G>A MANE Select	NP_000468.1:n.844-63G>A