Canonical Allele Identifier: CA357235254

Gene: ALB

Linked Data

• dbSNP Id: rs1718736378
• MyVariant Identifiers: chr4:g.74272348T>C (hg19) ; chr4:g.73406631T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406631T>C , CM000666.2:g.73406631T>C	GRCh38
NC_000004.11:g.74272348T>C , CM000666.1:g.74272348T>C	GRCh37
NC_000004.10:g.74491212T>C	NCBI36
NG_009291.1:g.7377T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.140T>C MANE Select	ENSP00000295897.4:p.Val47Ala
ENST00000295897.8:c.140T>C	ENSP00000295897.4:p.Val47Ala
ENST00000401494.7:c.137+1458T>C	ENSP00000384695.3:n.137+1458T>C
ENST00000415165.6:c.137+1458T>C	ENSP00000401820.2:n.137+1458T>C
ENST00000441319.5:c.146T>C	ENSP00000392541.1:p.Val49Ala
ENST00000476441.6:c.79+2225T>C	ENSP00000423727.1:n.79+2225T>C
ENST00000503124.5:c.-99T>C	ENSP00000421027.1:n.-99T>C
ENST00000509063.5:c.140T>C	ENSP00000422784.1:p.Val47Ala
ENST00000510166.5:n.176T>C
ENST00000514786.1:n.109T>C
ENST00000515133.5:n.181T>C
ENST00000621085.4:c.140T>C	ENSP00000483421.1:p.Val47Ala
ENST00000621628.4:c.140T>C	ENSP00000480485.1:p.Val47Ala
NM_000477.5:c.140T>C	NP_000468.1:p.Val47Ala
NM_000477.6:c.140T>C	NP_000468.1:p.Val47Ala
NM_000477.7:c.140T>C MANE Select	NP_000468.1:p.Val47Ala