Canonical Allele Identifier: CA2670844623
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670747-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670747C>A , CM000666.2:g.68670747C>A GRCh38
NC_000004.11:g.69536465C>A , CM000666.1:g.69536465C>A GRCh37
NC_000004.10:g.69219060C>A NCBI36
NG_052676.1:g.5030G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-129G>T NP_001067.2:n.-129G>T