Canonical Allele Identifier: CA2518111072
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404197G>T , CM000666.2:g.73404197G>T GRCh38
NC_000004.11:g.74269914G>T , CM000666.1:g.74269914G>T GRCh37
NC_000004.10:g.74488778G>T NCBI36
NG_009291.1:g.4943G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-172G>T ENSP00000392541.1:n.48-172G>T