Canonical Allele Identifier: CA2578063677
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404252del , CM000666.2:g.73404252del GRCh38
NC_000004.11:g.74269969del , CM000666.1:g.74269969del GRCh37
NC_000004.10:g.74488833del NCBI36
NG_009291.1:g.4998del

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-76del ENSP00000295897.4:n.-76del
ENST00000441319.5:c.48-117del ENSP00000392541.1:n.48-117del
NM_000477.6:c.-76del NP_000468.1:n.-76del