Canonical Allele Identifier: CA1466048838
Gene: UGT2B7 HGNC NCBI
UGT2B11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.69095621G>C , CM000666.2:g.69095621G>C GRCh38
NC_000004.11:g.69961339G>C , CM000666.1:g.69961339G>C GRCh37
NC_000004.10:g.69995928G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000502942.5:c.-26-2919G>C (UGT2B7) ENSP00000426206.1:n.-26-2919G>C
ENST00000509763.1:n.260-2919G>C (UGT2B7)
ENST00000615638.4:c.*106-90868C>G (UGT2B11) ENSP00000477842.1:n.*106-90868C>G
ENST00000620779.4:c.*380-90868C>G (UGT2B11) ENSP00000478182.1:n.*380-90868C>G
XM_005265702.2:c.-26-2919G>C (UGT2B7) XP_005265759.1:n.-26-2919G>C
XM_011532231.1:c.-26-2919G>C (UGT2B7) XP_011530533.1:n.-26-2919G>C
NM_001349568.1:c.-26-2919G>C (UGT2B7) NP_001336497.1:n.-26-2919G>C
NM_001349568.2:c.-26-2919G>C (UGT2B7) NP_001336497.1:n.-26-2919G>C
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