Canonical Allele Identifier: CA98760928
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs75779523
gnomAD v2: 4-69536472-A-C
gnomAD v3: 4-68670754-A-C
gnomAD v4: 4-68670754-A-C
MyVariant Identifiers: chr4:g.69536472A>C (hg19) chr4:g.68670754A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670754A>C , CM000666.2:g.68670754A>C GRCh38
NC_000004.11:g.69536472A>C , CM000666.1:g.69536472A>C GRCh37
NC_000004.10:g.69219067A>C NCBI36
NG_052676.1:g.5023T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-136T>G NP_001067.2:n.-136T>G
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