Canonical Allele Identifier: CA2670844622
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670744-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670744T>C , CM000666.2:g.68670744T>C GRCh38
NC_000004.11:g.69536462T>C , CM000666.1:g.69536462T>C GRCh37
NC_000004.10:g.69219057T>C NCBI36
NG_052676.1:g.5033A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-126A>G NP_001067.2:n.-126A>G