Canonical Allele Identifier: CA2552118011
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404170G>A , CM000666.2:g.73404170G>A GRCh38
NC_000004.11:g.74269887G>A , CM000666.1:g.74269887G>A GRCh37
NC_000004.10:g.74488751G>A NCBI36
NG_009291.1:g.4916G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-199G>A ENSP00000392541.1:n.48-199G>A