Canonical Allele Identifier: CA797795840
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1336587424
gnomAD v4: 4-68670762-C-T
MyVariant Identifiers: chr4:g.69536480C>T (hg19) chr4:g.68670762C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670762C>T , CM000666.2:g.68670762C>T GRCh38
NC_000004.11:g.69536480C>T , CM000666.1:g.69536480C>T GRCh37
NC_000004.10:g.69219075C>T NCBI36
NG_052676.1:g.5015G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-144G>A NP_001067.2:n.-144G>A
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