Canonical Allele Identifier: CA797795826
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1419324908
gnomAD v3: 4-68670720-A-G
gnomAD v4: 4-68670720-A-G
MyVariant Identifiers: chr4:g.69536438A>G (hg19) chr4:g.68670720A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670720A>G , CM000666.2:g.68670720A>G GRCh38
NC_000004.11:g.69536438A>G , CM000666.1:g.69536438A>G GRCh37
NC_000004.10:g.69219033A>G NCBI36
NG_052676.1:g.5057T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-102T>C NP_001067.2:n.-102T>C
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