Canonical Allele Identifier: CA2562054034
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404119T>A , CM000666.2:g.73404119T>A GRCh38
NC_000004.11:g.74269836T>A , CM000666.1:g.74269836T>A GRCh37
NC_000004.10:g.74488700T>A NCBI36
NG_009291.1:g.4865T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-250T>A ENSP00000392541.1:n.48-250T>A