Canonical Allele Identifier: CA2706083190

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs2109771897

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559925_68559926insATAT , CM000666.2:g.68559925_68559926insATAT	GRCh38
NC_000004.11:g.69425643_69425644insATAT , CM000666.1:g.69425643_69425644insATAT	GRCh37
NC_000004.10:g.69108238_69108239insATAT	NCBI36
NG_017033.1:g.13603_13604insTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+612_1005+613insTATA (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+612_1005+613insTATA
ENST00000684088.1:c.255+612_255+613insTATA (UGT2B17)	ENSP00000507374.1:n.255+612_255+613insTATA
ENST00000317746.2:c.1005+612_1005+613insTATA (UGT2B17)	ENSP00000320401.2:n.1005+612_1005+613insTATA
ENST00000616841.4:c.1733-22399_1733-22398insTATA (UGT2B15)	ENSP00000482004.1:n.1733-22399_1733-22398insTATA
NM_001077.3:c.1005+612_1005+613insTATA (UGT2B17)	NP_001068.1:n.1005+612_1005+613insTATA
XM_024454205.1:c.1005+612_1005+613insTATA (UGT2B17)	XP_024309973.1:n.1005+612_1005+613insTATA
NM_001077.4:c.1005+612_1005+613insTATA (UGT2B17) MANE Select	NP_001068.1:n.1005+612_1005+613insTATA