Canonical Allele Identifier: CA127879
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18185
ClinVar RCV Id: RCV000144686
dbSNP Id: rs74821926

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404398G>A , CM000666.2:g.73404398G>A GRCh38
NC_000004.11:g.74270115G>A , CM000666.1:g.74270115G>A GRCh37
NC_000004.10:g.74488979G>A NCBI36
NG_009291.1:g.5144G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.71G>A MANE Select ENSP00000295897.4:p.Arg24Gln
ENST00000295897.8:c.71G>A ENSP00000295897.4:p.Arg24Gln
ENST00000401494.7:c.71G>A ENSP00000384695.3:p.Arg24Gln
ENST00000415165.6:c.71G>A ENSP00000401820.2:p.Arg24Gln
ENST00000441319.5:n.77G>A ENSP00000392541.1:p.Arg26Gln
ENST00000476441.6:c.71G>A ENSP00000423727.1:p.Arg24Gln
ENST00000503124.5:c.-110G>A ENSP00000421027.1:n.-110G>A
ENST00000509063.5:c.71G>A ENSP00000422784.1:p.Arg24Gln
ENST00000510166.5:n.112G>A
ENST00000514786.1:n.48+62G>A
ENST00000515133.5:n.112G>A
ENST00000621085.4:c.71G>A ENSP00000483421.1:p.Arg24Gln
ENST00000621628.4:c.71G>A ENSP00000480485.1:p.Arg24Gln
NM_000477.5:c.71G>A NP_000468.1:p.Arg24Gln
NM_000477.6:c.71G>A NP_000468.1:p.Arg24Gln
NM_000477.7:c.71G>A MANE Select NP_000468.1:p.Arg24Gln