Canonical Allele Identifier: CA2670844632
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670761-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670761G>T , CM000666.2:g.68670761G>T GRCh38
NC_000004.11:g.69536479G>T , CM000666.1:g.69536479G>T GRCh37
NC_000004.10:g.69219074G>T NCBI36
NG_052676.1:g.5016C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-143C>A NP_001067.2:n.-143C>A