Canonical Allele Identifier: CA99696256
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs907562413
gnomAD v4: 4-73404237-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404237A>G , CM000666.2:g.73404237A>G GRCh38
NC_000004.11:g.74269954A>G , CM000666.1:g.74269954A>G GRCh37
NC_000004.10:g.74488818A>G NCBI36
NG_009291.1:g.4983A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-132A>G ENSP00000392541.1:n.48-132A>G