Canonical Allele Identifier: CA2670844599
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670688-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670688G>A , CM000666.2:g.68670688G>A GRCh38
NC_000004.11:g.69536406G>A , CM000666.1:g.69536406G>A GRCh37
NC_000004.10:g.69219001G>A NCBI36
NG_052676.1:g.5089C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-70C>T NP_001067.2:n.-70C>T