Canonical Allele Identifier: CA552304178
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1347454748
gnomAD v2: 4-74269814-C-A
gnomAD v3: 4-73404097-C-A
gnomAD v4: 4-73404097-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404097C>A , CM000666.2:g.73404097C>A GRCh38
NC_000004.11:g.74269814C>A , CM000666.1:g.74269814C>A GRCh37
NC_000004.10:g.74488678C>A NCBI36
NG_009291.1:g.4843C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-272C>A ENSP00000392541.1:n.48-272C>A