Canonical Allele Identifier: CA1468148360
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404237A= , CM000666.2:g.73404237A= GRCh38
NC_000004.11:g.74269954A= , CM000666.1:g.74269954A= GRCh37
NC_000004.10:g.74488818A= NCBI36
NG_009291.1:g.4983A=

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-132A= ENSP00000392541.1:n.48-132A=