Canonical Allele Identifier: CA2521178412
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404216G>A , CM000666.2:g.73404216G>A GRCh38
NC_000004.11:g.74269933G>A , CM000666.1:g.74269933G>A GRCh37
NC_000004.10:g.74488797G>A NCBI36
NG_009291.1:g.4962G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-153G>A ENSP00000392541.1:n.48-153G>A