Canonical Allele Identifier: CA1468148314
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404127G= , CM000666.2:g.73404127G= GRCh38
NC_000004.11:g.74269844G= , CM000666.1:g.74269844G= GRCh37
NC_000004.10:g.74488708G= NCBI36
NG_009291.1:g.4873G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-242G= ENSP00000392541.1:n.48-242G=