Canonical Allele Identifier: CA439800866

Gene: ALB

Linked Data

• dbSNP Id: rs962004
• MyVariant Identifiers: chr4:g.74285239C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419522C>A , CM000666.2:g.73419522C>A	GRCh38
NC_000004.11:g.74285239C>A , CM000666.1:g.74285239C>A	GRCh37
NC_000004.10:g.74504103C>A	NCBI36
NG_009291.1:g.20268C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1668C>A MANE Select	ENSP00000295897.4:p.Leu556=
ENST00000295897.8:c.1668C>A	ENSP00000295897.4:p.Leu556=
ENST00000401494.7:c.1323C>A	ENSP00000384695.3:p.Leu441=
ENST00000415165.6:c.1092C>A	ENSP00000401820.2:p.Leu364=
ENST00000476441.6:c.*947C>A	ENSP00000423727.1:n.*947C>A
ENST00000486939.1:n.322C>A
ENST00000503124.5:c.1218C>A	ENSP00000421027.1:p.Leu406=
ENST00000505649.5:n.1215C>A
ENST00000508932.5:n.175+67C>A
ENST00000509063.5:c.1668C>A	ENSP00000422784.1:p.Leu556=
ENST00000511370.1:c.1201C>A
ENST00000621085.4:c.1029C>A	ENSP00000483421.1:p.Leu343=
ENST00000621628.4:c.1029C>A	ENSP00000480485.1:p.Leu343=
NM_000477.5:c.1668C>A	NP_000468.1:p.Leu556=
NM_000477.6:c.1668C>A	NP_000468.1:p.Leu556=
NM_000477.7:c.1668C>A MANE Select	NP_000468.1:p.Leu556=