Canonical Allele Identifier: CA1468148331
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404171A= , CM000666.2:g.73404171A= GRCh38
NC_000004.11:g.74269888A= , CM000666.1:g.74269888A= GRCh37
NC_000004.10:g.74488752A= NCBI36
NG_009291.1:g.4917A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-198A= ENSP00000392541.1:n.48-198A=