Canonical Allele Identifier: CA2762177274
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404073T>C , CM000666.2:g.73404073T>C GRCh38
NC_000004.11:g.74269790T>C , CM000666.1:g.74269790T>C GRCh37
NC_000004.10:g.74488654T>C NCBI36
NG_009291.1:g.4819T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-296T>C ENSP00000392541.1:n.48-296T>C