Canonical Allele Identifier: CA98747408
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs780640445
MyVariant Identifiers: chr4:g.69512305T>C (hg19) chr4:g.68646587T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646587T>C , CM000666.2:g.68646587T>C GRCh38
NC_000004.11:g.69512305T>C , CM000666.1:g.69512305T>C GRCh37
NC_000004.10:g.69194900T>C NCBI36
NG_052676.1:g.29190A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+378A>G ENSP00000482004.1:n.1732+378A>G
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