Canonical Allele Identifier: CA357237520

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274506G>C (hg19) ; chr4:g.73408789G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408789G>C , CM000666.2:g.73408789G>C	GRCh38
NC_000004.11:g.74274506G>C , CM000666.1:g.74274506G>C	GRCh37
NC_000004.10:g.74493370G>C	NCBI36
NG_009291.1:g.9535G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.466G>C MANE Select	ENSP00000295897.4:p.Glu156Gln
ENST00000295897.8:c.466G>C	ENSP00000295897.4:p.Glu156Gln
ENST00000401494.7:c.138-566G>C	ENSP00000384695.3:n.138-566G>C
ENST00000415165.6:c.138-3207G>C	ENSP00000401820.2:n.138-3207G>C
ENST00000441319.5:c.472G>C	ENSP00000392541.1:p.Glu158Gln
ENST00000476441.6:c.80-566G>C	ENSP00000423727.1:n.80-566G>C
ENST00000503124.5:c.33-566G>C	ENSP00000421027.1:n.33-566G>C
ENST00000505649.5:n.152G>C
ENST00000509063.5:c.466G>C	ENSP00000422784.1:p.Glu156Gln
ENST00000510166.5:n.502G>C
ENST00000514786.1:n.435G>C
ENST00000515133.5:n.507G>C
ENST00000621085.4:c.466G>C	ENSP00000483421.1:p.Glu156Gln
ENST00000621628.4:c.466G>C	ENSP00000480485.1:p.Glu156Gln
NM_000477.5:c.466G>C	NP_000468.1:p.Glu156Gln
NM_000477.6:c.466G>C	NP_000468.1:p.Glu156Gln
NM_000477.7:c.466G>C MANE Select	NP_000468.1:p.Glu156Gln