Canonical Allele Identifier: CA170818
Gene: ALB HGNC NCBI

Linked Data

ClinVar Variation Id: 156314
ClinVar RCV Id: RCV000144398
dbSNP Id: rs75470261

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73406657C>T , CM000666.2:g.73406657C>T GRCh38
NC_000004.11:g.74272374C>T , CM000666.1:g.74272374C>T GRCh37
NC_000004.10:g.74491238C>T NCBI36
NG_009291.1:g.7403C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.166C>T MANE Select ENSP00000295897.4:p.Gln56Ter
ENST00000295897.8:c.166C>T ENSP00000295897.4:p.Gln56Ter
ENST00000401494.7:c.137+1484C>T ENSP00000384695.3:n.137+1484C>T
ENST00000415165.6:c.137+1484C>T ENSP00000401820.2:n.137+1484C>T
ENST00000441319.5:n.172C>T ENSP00000392541.1:p.Gln58Ter
ENST00000476441.6:c.79+2251C>T ENSP00000423727.1:n.79+2251C>T
ENST00000503124.5:c.-73C>T ENSP00000421027.1:n.-73C>T
ENST00000509063.5:c.166C>T ENSP00000422784.1:p.Gln56Ter
ENST00000510166.5:n.202C>T
ENST00000514786.1:n.135C>T
ENST00000515133.5:n.207C>T
ENST00000621085.4:c.166C>T ENSP00000483421.1:p.Gln56Ter
ENST00000621628.4:c.166C>T ENSP00000480485.1:p.Gln56Ter
NM_000477.5:c.166C>T NP_000468.1:p.Gln56Ter
NM_000477.6:c.166C>T NP_000468.1:p.Gln56Ter
NM_000477.7:c.166C>T MANE Select NP_000468.1:p.Gln56Ter