Canonical Allele Identifier: CA2670844627
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670750-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670750T>C , CM000666.2:g.68670750T>C GRCh38
NC_000004.11:g.69536468T>C , CM000666.1:g.69536468T>C GRCh37
NC_000004.10:g.69219063T>C NCBI36
NG_052676.1:g.5027A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-132A>G NP_001067.2:n.-132A>G