Canonical Allele Identifier: CA1465795089
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670719A= , CM000666.2:g.68670719A= GRCh38
NC_000004.11:g.69536437A= , CM000666.1:g.69536437A= GRCh37
NC_000004.10:g.69219032A= NCBI36
NG_052676.1:g.5058T=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-101T= NP_001067.2:n.-101T=