Canonical Allele Identifier: CA2670936384
Gene: ALB HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404219G>A , CM000666.2:g.73404219G>A GRCh38
NC_000004.11:g.74269936G>A , CM000666.1:g.74269936G>A GRCh37
NC_000004.10:g.74488800G>A NCBI36
NG_009291.1:g.4965G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-150G>A ENSP00000392541.1:n.48-150G>A