Canonical Allele Identifier: CA797795827
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1250723168
MyVariant Identifiers: chr4:g.69536449A>G (hg19) chr4:g.68670731A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670731A>G , CM000666.2:g.68670731A>G GRCh38
NC_000004.11:g.69536449A>G , CM000666.1:g.69536449A>G GRCh37
NC_000004.10:g.69219044A>G NCBI36
NG_052676.1:g.5046T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-113T>C NP_001067.2:n.-113T>C
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