Canonical Allele Identifier: CA1465795004
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670661C= , CM000666.2:g.68670661C= GRCh38
NC_000004.11:g.69536379C= , CM000666.1:g.69536379C= GRCh37
NC_000004.10:g.69218974C= NCBI36
NG_052676.1:g.5116G=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-43G= NP_001067.2:n.-43G=