Canonical Allele Identifier: CA1468148308
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404117A= , CM000666.2:g.73404117A= GRCh38
NC_000004.11:g.74269834A= , CM000666.1:g.74269834A= GRCh37
NC_000004.10:g.74488698A= NCBI36
NG_009291.1:g.4863A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-252A= ENSP00000392541.1:n.48-252A=