Canonical Allele Identifier: CA1465795118
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670754A= , CM000666.2:g.68670754A= GRCh38
NC_000004.11:g.69536472A= , CM000666.1:g.69536472A= GRCh37
NC_000004.10:g.69219067A= NCBI36
NG_052676.1:g.5023T=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-136T= NP_001067.2:n.-136T=