Canonical Allele Identifier: CA1465795034
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670665C= , CM000666.2:g.68670665C= GRCh38
NC_000004.11:g.69536383C= , CM000666.1:g.69536383C= GRCh37
NC_000004.10:g.69218978C= NCBI36
NG_052676.1:g.5112G=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-47G= NP_001067.2:n.-47G=