Canonical Allele Identifier: CA1465795109
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1560613790

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670744T>A , CM000666.2:g.68670744T>A GRCh38
NC_000004.11:g.69536462T>A , CM000666.1:g.69536462T>A GRCh37
NC_000004.10:g.69219057T>A NCBI36
NG_052676.1:g.5033A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-126A>T NP_001067.2:n.-126A>T