Canonical Allele Identifier: CA1468148333
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404178T= , CM000666.2:g.73404178T= GRCh38
NC_000004.11:g.74269895T= , CM000666.1:g.74269895T= GRCh37
NC_000004.10:g.74488759T= NCBI36
NG_009291.1:g.4924T=

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-191T= ENSP00000392541.1:n.48-191T=