Canonical Allele Identifier: CA1465820656

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1732473961

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646583T>C , CM000666.2:g.68646583T>C	GRCh38
NC_000004.11:g.69512301T>C , CM000666.1:g.69512301T>C	GRCh37
NC_000004.10:g.69194896T>C	NCBI36
NG_052676.1:g.29194A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616841.4:c.1732+382A>G	ENSP00000482004.1:n.1732+382A>G