Canonical Allele Identifier: CA2548492033
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670698-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670698T>G , CM000666.2:g.68670698T>G GRCh38
NC_000004.11:g.69536416T>G , CM000666.1:g.69536416T>G GRCh37
NC_000004.10:g.69219011T>G NCBI36
NG_052676.1:g.5079A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-80A>C NP_001067.2:n.-80A>C