Canonical Allele Identifier: CA2942808
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs779030008

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670659_68670662del , CM000666.2:g.68670659_68670662del GRCh38
NC_000004.11:g.69536377_69536380del , CM000666.1:g.69536377_69536380del GRCh37
NC_000004.10:g.69218972_69218975del NCBI36
NG_052676.1:g.5120_5123del

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-39_-36del NP_001067.2:n.-39_-36del