Canonical Allele Identifier: CA797795845
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1408443791
gnomAD v4: 4-68670775-C-T
MyVariant Identifiers: chr4:g.69536493C>T (hg19) chr4:g.68670775C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670775C>T , CM000666.2:g.68670775C>T GRCh38
NC_000004.11:g.69536493C>T , CM000666.1:g.69536493C>T GRCh37
NC_000004.10:g.69219088C>T NCBI36
NG_052676.1:g.5002G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-157G>A NP_001067.2:n.-157G>A
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