Canonical Allele Identifier: CA1466049196

Gene: UGT2B7 UGT2B11

Linked Data

• dbSNP Id: rs7668258

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.69096360T>G , CM000666.2:g.69096360T>G	GRCh38
NC_000004.11:g.69962078T>G , CM000666.1:g.69962078T>G	GRCh37
NC_000004.10:g.69996667T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502942.5:c.-26-2180T>G (UGT2B7)	ENSP00000426206.1:n.-26-2180T>G
ENST00000509763.1:n.260-2180T>G (UGT2B7)
ENST00000615638.4:c.*106-91607A>C (UGT2B11)	ENSP00000477842.1:n.*106-91607A>C
ENST00000620779.4:c.*380-91607A>C (UGT2B11)	ENSP00000478182.1:n.*380-91607A>C
XM_005265702.2:c.-26-2180T>G (UGT2B7)	XP_005265759.1:n.-26-2180T>G
XM_011532231.1:c.-26-2180T>G (UGT2B7)	XP_011530533.1:n.-26-2180T>G
NM_001349568.1:c.-26-2180T>G (UGT2B7)	NP_001336497.1:n.-26-2180T>G
NM_001349568.2:c.-26-2180T>G (UGT2B7)	NP_001336497.1:n.-26-2180T>G