Canonical Allele Identifier: CA1468148330
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404165G= , CM000666.2:g.73404165G= GRCh38
NC_000004.11:g.74269882G= , CM000666.1:g.74269882G= GRCh37
NC_000004.10:g.74488746G= NCBI36
NG_009291.1:g.4911G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-204G= ENSP00000392541.1:n.48-204G=