Canonical Allele Identifier: CA552185669
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1340308301
gnomAD v2: 4-69536392-T-G
gnomAD v3: 4-68670674-T-G
gnomAD v4: 4-68670674-T-G
MyVariant Identifiers: chr4:g.69536392T>G (hg19) chr4:g.68670674T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670674T>G , CM000666.2:g.68670674T>G GRCh38
NC_000004.11:g.69536392T>G , CM000666.1:g.69536392T>G GRCh37
NC_000004.10:g.69218987T>G NCBI36
NG_052676.1:g.5103A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-56A>C NP_001067.2:n.-56A>C
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