Canonical Allele Identifier: CA797835093

Gene: UGT2B7 UGT2B11

Linked Data

• dbSNP Id: rs1199283610
• gnomAD v3: 4-69096325-TC-T
• gnomAD v4: 4-69096325-TC-T
• MyVariant Identifiers: chr4:g.69962044del (hg19) ; chr4:g.69096326del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.69096326del , CM000666.2:g.69096326del	GRCh38
NC_000004.11:g.69962044del , CM000666.1:g.69962044del	GRCh37
NC_000004.10:g.69996633del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502942.5:c.-26-2214del (UGT2B7)	ENSP00000426206.1:n.-26-2214del
ENST00000509763.1:n.260-2214del (UGT2B7)
ENST00000615638.4:c.*106-91573del (UGT2B11)	ENSP00000477842.1:n.*106-91573del
ENST00000620779.4:c.*380-91573del (UGT2B11)	ENSP00000478182.1:n.*380-91573del
XM_005265702.2:c.-26-2214del (UGT2B7)	XP_005265759.1:n.-26-2214del
XM_011532231.1:c.-26-2214del (UGT2B7)	XP_011530533.1:n.-26-2214del
NM_001349568.1:c.-26-2214del (UGT2B7)	NP_001336497.1:n.-26-2214del
NM_001349568.2:c.-26-2214del (UGT2B7)	NP_001336497.1:n.-26-2214del