Canonical Allele Identifier: CA2670844583
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670654-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670654T>C , CM000666.2:g.68670654T>C GRCh38
NC_000004.11:g.69536372T>C , CM000666.1:g.69536372T>C GRCh37
NC_000004.10:g.69218967T>C NCBI36
NG_052676.1:g.5123A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-36A>G NP_001067.2:n.-36A>G