Canonical Allele Identifier: CA1468148303
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404105T= , CM000666.2:g.73404105T= GRCh38
NC_000004.11:g.74269822T= , CM000666.1:g.74269822T= GRCh37
NC_000004.10:g.74488686T= NCBI36
NG_009291.1:g.4851T=

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-264T= ENSP00000392541.1:n.48-264T=