Canonical Allele Identifier: CA2670844613
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670722-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670722A>G , CM000666.2:g.68670722A>G GRCh38
NC_000004.11:g.69536440A>G , CM000666.1:g.69536440A>G GRCh37
NC_000004.10:g.69219035A>G NCBI36
NG_052676.1:g.5055T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-104T>C NP_001067.2:n.-104T>C