Canonical Allele Identifier: CA797795829
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1486604737
MyVariant Identifiers: chr4:g.69536468T>A (hg19) chr4:g.68670750T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670750T>A , CM000666.2:g.68670750T>A GRCh38
NC_000004.11:g.69536468T>A , CM000666.1:g.69536468T>A GRCh37
NC_000004.10:g.69219063T>A NCBI36
NG_052676.1:g.5027A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-132A>T NP_001067.2:n.-132A>T
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