Canonical Allele Identifier: CA2670936381
Gene: ALB HGNC NCBI

Linked Data

gnomAD v4: 4-73404212-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404212C>G , CM000666.2:g.73404212C>G GRCh38
NC_000004.11:g.74269929C>G , CM000666.1:g.74269929C>G GRCh37
NC_000004.10:g.74488793C>G NCBI36
NG_009291.1:g.4958C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-157C>G ENSP00000392541.1:n.48-157C>G