Canonical Allele Identifier: CA1465795126
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670760T= , CM000666.2:g.68670760T= GRCh38
NC_000004.11:g.69536478T= , CM000666.1:g.69536478T= GRCh37
NC_000004.10:g.69219073T= NCBI36
NG_052676.1:g.5017A=

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-142A= NP_001067.2:n.-142A=