Canonical Allele Identifier: CA1465795068
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670702G= , CM000666.2:g.68670702G= GRCh38
NC_000004.11:g.69536420G= , CM000666.1:g.69536420G= GRCh37
NC_000004.10:g.69219015G= NCBI36
NG_052676.1:g.5075C=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-84C= NP_001067.2:n.-84C=