Canonical Allele Identifier: CA552185671
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1225672915
gnomAD v2: 4-69536420-G-T
gnomAD v3: 4-68670702-G-T
gnomAD v4: 4-68670702-G-T
MyVariant Identifiers: chr4:g.69536420G>T (hg19) chr4:g.68670702G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670702G>T , CM000666.2:g.68670702G>T GRCh38
NC_000004.11:g.69536420G>T , CM000666.1:g.69536420G>T GRCh37
NC_000004.10:g.69219015G>T NCBI36
NG_052676.1:g.5075C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-84C>A NP_001067.2:n.-84C>A
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