Canonical Allele Identifier: CA2670844636
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670765-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670765G>A , CM000666.2:g.68670765G>A GRCh38
NC_000004.11:g.69536483G>A , CM000666.1:g.69536483G>A GRCh37
NC_000004.10:g.69219078G>A NCBI36
NG_052676.1:g.5012C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-147C>T NP_001067.2:n.-147C>T