Canonical Allele Identifier: CA127960
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18230
ClinVar RCV Id: RCV000019891
dbSNP Id: rs78283180

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73409363A>G , CM000666.2:g.73409363A>G GRCh38
NC_000004.11:g.74275080A>G , CM000666.1:g.74275080A>G GRCh37
NC_000004.10:g.74493944A>G NCBI36
NG_009291.1:g.10109A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.491A>G MANE Select ENSP00000295897.4:p.Tyr164Cys
ENST00000295897.8:c.491A>G ENSP00000295897.4:p.Tyr164Cys
ENST00000401494.7:c.146A>G ENSP00000384695.3:p.Tyr49Cys
ENST00000415165.6:c.138-2633A>G ENSP00000401820.2:n.138-2633A>G
ENST00000441319.5:n.497A>G ENSP00000392541.1:p.Tyr166Cys
ENST00000476441.6:c.88A>G ENSP00000423727.1:p.Met30Val
ENST00000503124.5:c.41A>G ENSP00000421027.1:p.Tyr14Cys
ENST00000505649.5:n.177A>G
ENST00000509063.5:c.491A>G ENSP00000422784.1:p.Tyr164Cys
ENST00000511370.1:n.24A>G
ENST00000514786.1:n.460A>G
ENST00000621085.4:c.490+1A>G ENSP00000483421.1:n.490+1A>G
ENST00000621628.4:c.486+287A>G ENSP00000480485.1:n.486+287A>G
NM_000477.5:c.491A>G NP_000468.1:p.Tyr164Cys
NM_000477.6:c.491A>G NP_000468.1:p.Tyr164Cys
NM_000477.7:c.491A>G MANE Select NP_000468.1:p.Tyr164Cys