Canonical Allele Identifier: CA1468148315
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404134A= , CM000666.2:g.73404134A= GRCh38
NC_000004.11:g.74269851A= , CM000666.1:g.74269851A= GRCh37
NC_000004.10:g.74488715A= NCBI36
NG_009291.1:g.4880A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-235A= ENSP00000392541.1:n.48-235A=