Canonical Allele Identifier: CA2670936353
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404167C>A , CM000666.2:g.73404167C>A GRCh38
NC_000004.11:g.74269884C>A , CM000666.1:g.74269884C>A GRCh37
NC_000004.10:g.74488748C>A NCBI36
NG_009291.1:g.4913C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-202C>A ENSP00000392541.1:n.48-202C>A