Canonical Allele Identifier: CA2942810
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs565672689
ExAC: 4:69536379 C / T
gnomAD v2: 4-69536379-C-T
gnomAD v3: 4-68670661-C-T
gnomAD v4: 4-68670661-C-T
MyVariant Identifiers: chr4:g.69536379C>T (hg19) chr4:g.68670661C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670661C>T , CM000666.2:g.68670661C>T GRCh38
NC_000004.11:g.69536379C>T , CM000666.1:g.69536379C>T GRCh37
NC_000004.10:g.69218974C>T NCBI36
NG_052676.1:g.5116G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-43G>A NP_001067.2:n.-43G>A
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