Canonical Allele Identifier: CA2762177278
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404168A>G , CM000666.2:g.73404168A>G GRCh38
NC_000004.11:g.74269885A>G , CM000666.1:g.74269885A>G GRCh37
NC_000004.10:g.74488749A>G NCBI36
NG_009291.1:g.4914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-201A>G ENSP00000392541.1:n.48-201A>G