Canonical Allele Identifier: CA127890
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18191
ClinVar RCV Id: RCV000019833
dbSNP Id: rs79744198

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73413454A>G , CM000666.2:g.73413454A>G GRCh38
NC_000004.11:g.74279171A>G , CM000666.1:g.74279171A>G GRCh37
NC_000004.10:g.74498035A>G NCBI36
NG_009291.1:g.14200A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.878A>G MANE Select ENSP00000295897.4:p.Asp293Gly
ENST00000295897.8:c.878A>G ENSP00000295897.4:p.Asp293Gly
ENST00000401494.7:c.533A>G ENSP00000384695.3:p.Asp178Gly
ENST00000415165.6:c.302A>G ENSP00000401820.2:p.Asp101Gly
ENST00000476441.6:c.*157A>G ENSP00000423727.1:p.=
ENST00000484992.1:n.198A>G
ENST00000503124.5:c.428A>G ENSP00000421027.1:p.Asp143Gly
ENST00000505649.5:n.564A>G
ENST00000509063.5:c.878A>G ENSP00000422784.1:p.Asp293Gly
ENST00000511370.1:n.411A>G
ENST00000621085.4:c.491-1652A>G ENSP00000483421.1:p.=
ENST00000621628.4:c.487-1648A>G ENSP00000480485.1:p.=
NM_000477.5:c.878A>G NP_000468.1:p.Asp293Gly
NM_000477.6:c.878A>G NP_000468.1:p.Asp293Gly
NM_000477.7:c.878A>G MANE Select NP_000468.1:p.Asp293Gly