Canonical Allele Identifier: CA798282522
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1267013031

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404060del , CM000666.2:g.73404060del GRCh38
NC_000004.11:g.74269777del , CM000666.1:g.74269777del GRCh37
NC_000004.10:g.74488641del NCBI36
NG_009291.1:g.4806del

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-309del ENSP00000392541.1:n.48-309del