Canonical Allele Identifier: CA1465883993
Gene: UGT2B10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68817181T= , CM000666.2:g.68817181T= GRCh38
NC_000004.11:g.69682899T= , CM000666.1:g.69682899T= GRCh37
NC_000004.10:g.69717488T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+444T= MANE Select ENSP00000265403.7:n.718+444T=
ENST00000265403.11:c.718+444T= ENSP00000265403.7:n.718+444T=
ENST00000458688.2:c.466+696T= ENSP00000413420.2:n.466+696T=
NM_001075.5:c.718+444T= NP_001066.1:n.718+444T=
NM_001144767.2:c.466+696T= NP_001138239.1:n.466+696T=
NM_001290091.1:c.-26-848T= NP_001277020.1:n.-26-848T=
XM_017008585.2:c.718+444T= XP_016864074.1:n.718+444T=
NM_001075.6:c.718+444T= MANE Select NP_001066.1:n.718+444T=
NM_001144767.3:c.466+696T= NP_001138239.1:n.466+696T=
NM_001290091.2:c.-26-848T= NP_001277020.1:n.-26-848T=
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