Canonical Allele Identifier: CA2762061375
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670756T>C , CM000666.2:g.68670756T>C GRCh38
NC_000004.11:g.69536474T>C , CM000666.1:g.69536474T>C GRCh37
NC_000004.10:g.69219069T>C NCBI36
NG_052676.1:g.5021A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-138A>G NP_001067.2:n.-138A>G