Canonical Allele Identifier: CA1465820659

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1560600719

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646591A>G , CM000666.2:g.68646591A>G	GRCh38
NC_000004.11:g.69512309A>G , CM000666.1:g.69512309A>G	GRCh37
NC_000004.10:g.69194904A>G	NCBI36
NG_052676.1:g.29186T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616841.4:c.1732+374T>C	ENSP00000482004.1:n.1732+374T>C