Canonical Allele Identifier: CA1465795066
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670698T= , CM000666.2:g.68670698T= GRCh38
NC_000004.11:g.69536416T= , CM000666.1:g.69536416T= GRCh37
NC_000004.10:g.69219011T= NCBI36
NG_052676.1:g.5079A=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-80A= NP_001067.2:n.-80A=