Canonical Allele Identifier: CA2670844626
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670749-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670749G>T , CM000666.2:g.68670749G>T GRCh38
NC_000004.11:g.69536467G>T , CM000666.1:g.69536467G>T GRCh37
NC_000004.10:g.69219062G>T NCBI36
NG_052676.1:g.5028C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-131C>A NP_001067.2:n.-131C>A