Canonical Allele Identifier: CA2670844608
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670707-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670707A>C , CM000666.2:g.68670707A>C GRCh38
NC_000004.11:g.69536425A>C , CM000666.1:g.69536425A>C GRCh37
NC_000004.10:g.69219020A>C NCBI36
NG_052676.1:g.5070T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-89T>G NP_001067.2:n.-89T>G