Canonical Allele Identifier: CA1465820661
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732474133
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646592G>A , CM000666.2:g.68646592G>A GRCh38
NC_000004.11:g.69512310G>A , CM000666.1:g.69512310G>A GRCh37
NC_000004.10:g.69194905G>A NCBI36
NG_052676.1:g.29185C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+373C>T ENSP00000482004.1:n.1732+373C>T
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