Canonical Allele Identifier: CA2670936340
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404150G>A , CM000666.2:g.73404150G>A GRCh38
NC_000004.11:g.74269867G>A , CM000666.1:g.74269867G>A GRCh37
NC_000004.10:g.74488731G>A NCBI36
NG_009291.1:g.4896G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-219G>A ENSP00000392541.1:n.48-219G>A