Canonical Allele Identifier: CA2944517
Gene: UGT2B7 HGNC NCBI
UGT2B11 HGNC NCBI

Linked Data

ClinVar Variation Id: 718812
dbSNP Id: rs61361928
gnomAD v2: 4-69962375-T-C
gnomAD v3: 4-69096657-T-C
gnomAD v4: 4-69096657-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69096657T>C , CM000666.2:g.69096657T>C GRCh38
NC_000004.11:g.69962375T>C , CM000666.1:g.69962375T>C GRCh37
NC_000004.10:g.69996964T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305231.12:c.137T>C (UGT2B7) MANE Select ENSP00000304811.7:p.Leu46Pro
ENST00000305231.11:c.137T>C (UGT2B7) ENSP00000304811.7:p.Leu46Pro
ENST00000502942.5:c.-26-1883T>C (UGT2B7) ENSP00000426206.1:n.-26-1883T>C
ENST00000508661.5:c.137T>C (UGT2B7) ENSP00000427659.1:p.Leu46Pro
ENST00000509763.1:n.260-1883T>C (UGT2B7)
ENST00000615638.4:c.*106-91904A>G (UGT2B11) ENSP00000477842.1:n.*106-91904A>G
ENST00000620779.4:c.*380-91904A>G (UGT2B11) ENSP00000478182.1:n.*380-91904A>G
ENST00000622664.1:c.137T>C (UGT2B7) ENSP00000483172.1:p.Leu46Pro
NM_001074.2:c.137T>C (UGT2B7) NP_001065.2:p.Leu46Pro
XM_005265702.2:c.-26-1883T>C (UGT2B7) XP_005265759.1:n.-26-1883T>C
XM_011532229.1:c.137T>C (UGT2B7) XP_011530531.1:p.Leu46Pro
XM_011532230.1:c.137T>C (UGT2B7) XP_011530532.1:p.Leu46Pro
XM_011532231.1:c.-26-1883T>C (UGT2B7) XP_011530533.1:n.-26-1883T>C
NM_001074.3:c.137T>C (UGT2B7) NP_001065.2:p.Leu46Pro
NM_001330719.1:c.137T>C (UGT2B7) NP_001317648.1:p.Leu46Pro
NM_001349568.1:c.-26-1883T>C (UGT2B7) NP_001336497.1:n.-26-1883T>C
XM_011532229.2:c.137T>C (UGT2B7) XP_011530531.1:p.Leu46Pro
NM_001074.4:c.137T>C (UGT2B7) MANE Select NP_001065.2:p.Leu46Pro
NM_001330719.2:c.137T>C (UGT2B7) NP_001317648.1:p.Leu46Pro
NM_001349568.2:c.-26-1883T>C (UGT2B7) NP_001336497.1:n.-26-1883T>C