Canonical Allele Identifier: CA2552501939
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404158A>C , CM000666.2:g.73404158A>C GRCh38
NC_000004.11:g.74269875A>C , CM000666.1:g.74269875A>C GRCh37
NC_000004.10:g.74488739A>C NCBI36
NG_009291.1:g.4904A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-211A>C ENSP00000392541.1:n.48-211A>C