Canonical Allele Identifier: CA127883
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 18187
ClinVar RCV Id: RCV000144688
dbSNP Id: rs75353611

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404401A>T , CM000666.2:g.73404401A>T GRCh38
NC_000004.11:g.74270118A>T , CM000666.1:g.74270118A>T GRCh37
NC_000004.10:g.74488982A>T NCBI36
NG_009291.1:g.5147A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.74A>T MANE Select ENSP00000295897.4:p.Asp25Val
ENST00000295897.8:c.74A>T ENSP00000295897.4:p.Asp25Val
ENST00000401494.7:c.74A>T ENSP00000384695.3:p.Asp25Val
ENST00000415165.6:c.74A>T ENSP00000401820.2:p.Asp25Val
ENST00000441319.5:n.80A>T ENSP00000392541.1:p.Asp27Val
ENST00000476441.6:c.74A>T ENSP00000423727.1:p.Asp25Val
ENST00000503124.5:c.-107A>T ENSP00000421027.1:n.-107A>T
ENST00000509063.5:c.74A>T ENSP00000422784.1:p.Asp25Val
ENST00000510166.5:n.115A>T
ENST00000514786.1:n.48+65A>T
ENST00000515133.5:n.115A>T
ENST00000621085.4:c.74A>T ENSP00000483421.1:p.Asp25Val
ENST00000621628.4:c.74A>T ENSP00000480485.1:p.Asp25Val
NM_000477.5:c.74A>T NP_000468.1:p.Asp25Val
NM_000477.6:c.74A>T NP_000468.1:p.Asp25Val
NM_000477.7:c.74A>T MANE Select NP_000468.1:p.Asp25Val