Canonical Allele Identifier: CA439800266

Gene: ALB

Linked Data

• dbSNP Id: rs760686684
• gnomAD v4: 4-73415059-G-A
• MyVariant Identifiers: chr4:g.74280776G>A (hg19) ; chr4:g.73415059G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415059G>A , CM000666.2:g.73415059G>A	GRCh38
NC_000004.11:g.74280776G>A , CM000666.1:g.74280776G>A	GRCh37
NC_000004.10:g.74499640G>A	NCBI36
NG_009291.1:g.15805G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1083G>A MANE Select	ENSP00000295897.4:p.Arg361=
ENST00000295897.8:c.1083G>A	ENSP00000295897.4:p.Arg361=
ENST00000401494.7:c.738G>A	ENSP00000384695.3:p.Arg246=
ENST00000415165.6:c.507G>A	ENSP00000401820.2:p.Arg169=
ENST00000476441.6:c.*362G>A	ENSP00000423727.1:n.*362G>A
ENST00000484992.1:n.403G>A
ENST00000503124.5:c.633G>A	ENSP00000421027.1:p.Arg211=
ENST00000504043.1:n.86G>A
ENST00000505649.5:n.769G>A
ENST00000509063.5:c.1083G>A	ENSP00000422784.1:p.Arg361=
ENST00000511370.1:c.616G>A
ENST00000621085.4:c.491-47G>A	ENSP00000483421.1:n.491-47G>A
ENST00000621628.4:c.487-43G>A	ENSP00000480485.1:n.487-43G>A
NM_000477.5:c.1083G>A	NP_000468.1:p.Arg361=
NM_000477.6:c.1083G>A	NP_000468.1:p.Arg361=
NM_000477.7:c.1083G>A MANE Select	NP_000468.1:p.Arg361=