Canonical Allele Identifier: CA1465771025

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1731220571

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68567494G>T , CM000666.2:g.68567494G>T	GRCh38
NC_000004.11:g.69433212G>T , CM000666.1:g.69433212G>T	GRCh37
NC_000004.10:g.69115807G>T	NCBI36
NG_017033.1:g.6034C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.724+267C>A (UGT2B17) MANE Select	ENSP00000320401.2:n.724+267C>A
ENST00000684088.1:c.-26-1774C>A (UGT2B17)	ENSP00000507374.1:n.-26-1774C>A
ENST00000317746.2:c.724+267C>A (UGT2B17)	ENSP00000320401.2:n.724+267C>A
ENST00000616841.4:c.1733-29968C>A (UGT2B15)	ENSP00000482004.1:n.1733-29968C>A
NM_001077.3:c.724+267C>A (UGT2B17)	NP_001068.1:n.724+267C>A
XM_024454205.1:c.724+267C>A (UGT2B17)	XP_024309973.1:n.724+267C>A
NM_001077.4:c.724+267C>A (UGT2B17) MANE Select	NP_001068.1:n.724+267C>A