Canonical Allele Identifier: CA1468148321
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404143G= , CM000666.2:g.73404143G= GRCh38
NC_000004.11:g.74269860G= , CM000666.1:g.74269860G= GRCh37
NC_000004.10:g.74488724G= NCBI36
NG_009291.1:g.4889G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-226G= ENSP00000392541.1:n.48-226G=