Canonical Allele Identifier: CA98760923
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1039425797
gnomAD v2: 4-69536459-T-C
gnomAD v3: 4-68670741-T-C
gnomAD v4: 4-68670741-T-C
MyVariant Identifiers: chr4:g.69536459T>C (hg19) chr4:g.68670741T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670741T>C , CM000666.2:g.68670741T>C GRCh38
NC_000004.11:g.69536459T>C , CM000666.1:g.69536459T>C GRCh37
NC_000004.10:g.69219054T>C NCBI36
NG_052676.1:g.5036A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-123A>G NP_001067.2:n.-123A>G
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