Canonical Allele Identifier: CA1465795119
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670755A= , CM000666.2:g.68670755A= GRCh38
NC_000004.11:g.69536473A= , CM000666.1:g.69536473A= GRCh37
NC_000004.10:g.69219068A= NCBI36
NG_052676.1:g.5022T=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-137T= NP_001067.2:n.-137T=