Canonical Allele Identifier: CA1064137029
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404141A>G , CM000666.2:g.73404141A>G GRCh38
NC_000004.11:g.74269858A>G , CM000666.1:g.74269858A>G GRCh37
NC_000004.10:g.74488722A>G NCBI36
NG_009291.1:g.4887A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-228A>G ENSP00000392541.1:n.48-228A>G