Canonical Allele Identifier: CA357247012

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285971G>C (hg19) ; chr4:g.73420254G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420254G>C , CM000666.2:g.73420254G>C	GRCh38
NC_000004.11:g.74285971G>C , CM000666.1:g.74285971G>C	GRCh37
NC_000004.10:g.74504835G>C	NCBI36
NG_009291.1:g.21000G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786G>C MANE Select	ENSP00000295897.4:p.Gly596Arg
ENST00000295897.8:c.1786G>C	ENSP00000295897.4:p.Gly596Arg
ENST00000401494.7:c.1441G>C	ENSP00000384695.3:p.Gly481Arg
ENST00000415165.6:c.1210G>C	ENSP00000401820.2:p.Gly404Arg
ENST00000476441.6:c.*1065G>C	ENSP00000423727.1:n.*1065G>C
ENST00000495173.1:n.94G>C
ENST00000503124.5:c.1336G>C	ENSP00000421027.1:p.Gly446Arg
ENST00000505649.5:n.1333G>C
ENST00000508932.5:n.176G>C
ENST00000509063.5:c.1785+615G>C	ENSP00000422784.1:n.1785+615G>C
ENST00000511370.1:c.1319G>C
ENST00000621085.4:c.1147G>C	ENSP00000483421.1:p.Gly383Arg
ENST00000621628.4:c.1147G>C	ENSP00000480485.1:p.Gly383Arg
NM_000477.5:c.1786G>C	NP_000468.1:p.Gly596Arg
NM_000477.6:c.1786G>C	NP_000468.1:p.Gly596Arg
NM_000477.7:c.1786G>C MANE Select	NP_000468.1:p.Gly596Arg