Canonical Allele Identifier: CA357244978

Gene: ALB

Linked Data

• dbSNP Id: rs74826639
• MyVariant Identifiers: chr4:g.74283961G>C (hg19) ; chr4:g.73418244G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418244G>C , CM000666.2:g.73418244G>C	GRCh38
NC_000004.11:g.74283961G>C , CM000666.1:g.74283961G>C	GRCh37
NC_000004.10:g.74502825G>C	NCBI36
NG_009291.1:g.18990G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1585G>C MANE Select	ENSP00000295897.4:p.Glu529Gln
ENST00000295897.8:c.1585G>C	ENSP00000295897.4:p.Glu529Gln
ENST00000401494.7:c.1240G>C	ENSP00000384695.3:p.Glu414Gln
ENST00000415165.6:c.1009G>C	ENSP00000401820.2:p.Glu337Gln
ENST00000476441.6:c.*864G>C	ENSP00000423727.1:n.*864G>C
ENST00000486939.1:n.239G>C
ENST00000503124.5:c.1135G>C	ENSP00000421027.1:p.Glu379Gln
ENST00000505649.5:n.1132G>C
ENST00000509063.5:c.1585G>C	ENSP00000422784.1:p.Glu529Gln
ENST00000511370.1:c.1118G>C
ENST00000621085.4:c.946G>C	ENSP00000483421.1:p.Glu316Gln
ENST00000621628.4:c.946G>C	ENSP00000480485.1:p.Glu316Gln
NM_000477.5:c.1585G>C	NP_000468.1:p.Glu529Gln
NM_000477.6:c.1585G>C	NP_000468.1:p.Glu529Gln
NM_000477.7:c.1585G>C MANE Select	NP_000468.1:p.Glu529Gln