Canonical Allele Identifier: CA1465795079
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670709T= , CM000666.2:g.68670709T= GRCh38
NC_000004.11:g.69536427T= , CM000666.1:g.69536427T= GRCh37
NC_000004.10:g.69219022T= NCBI36
NG_052676.1:g.5068A=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-91A= NP_001067.2:n.-91A=