Canonical Allele Identifier: CA2959749

Gene: ALB

Linked Data

• dbSNP Id: rs753424895
• ExAC: 4:74285972 G / C
• gnomAD v2: 4-74285972-G-C
• gnomAD v3: 4-73420255-G-C
• gnomAD v4: 4-73420255-G-C
• MyVariant Identifiers: chr4:g.74285972G>C (hg19) ; chr4:g.73420255G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420255G>C , CM000666.2:g.73420255G>C	GRCh38
NC_000004.11:g.74285972G>C , CM000666.1:g.74285972G>C	GRCh37
NC_000004.10:g.74504836G>C	NCBI36
NG_009291.1:g.21001G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1787G>C MANE Select	ENSP00000295897.4:p.Gly596Ala
ENST00000295897.8:c.1787G>C	ENSP00000295897.4:p.Gly596Ala
ENST00000401494.7:c.1442G>C	ENSP00000384695.3:p.Gly481Ala
ENST00000415165.6:c.1211G>C	ENSP00000401820.2:p.Gly404Ala
ENST00000476441.6:c.*1066G>C	ENSP00000423727.1:n.*1066G>C
ENST00000495173.1:n.95G>C
ENST00000503124.5:c.1337G>C	ENSP00000421027.1:p.Gly446Ala
ENST00000505649.5:n.1334G>C
ENST00000508932.5:n.177G>C
ENST00000509063.5:c.1785+616G>C	ENSP00000422784.1:n.1785+616G>C
ENST00000511370.1:c.1320G>C
ENST00000621085.4:c.1148G>C	ENSP00000483421.1:p.Gly383Ala
ENST00000621628.4:c.1148G>C	ENSP00000480485.1:p.Gly383Ala
NM_000477.5:c.1787G>C	NP_000468.1:p.Gly596Ala
NM_000477.6:c.1787G>C	NP_000468.1:p.Gly596Ala
NM_000477.7:c.1787G>C MANE Select	NP_000468.1:p.Gly596Ala