Canonical Allele Identifier: CA1465884065
Gene: UGT2B10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68817312T= , CM000666.2:g.68817312T= GRCh38
NC_000004.11:g.69683030T= , CM000666.1:g.69683030T= GRCh37
NC_000004.10:g.69717619T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+575T= MANE Select ENSP00000265403.7:n.718+575T=
ENST00000265403.11:c.718+575T= ENSP00000265403.7:n.718+575T=
ENST00000458688.2:c.467-717T= ENSP00000413420.2:n.467-717T=
NM_001075.5:c.718+575T= NP_001066.1:n.718+575T=
NM_001144767.2:c.467-717T= NP_001138239.1:n.467-717T=
NM_001290091.1:c.-26-717T= NP_001277020.1:n.-26-717T=
XM_017008585.2:c.718+575T= XP_016864074.1:n.718+575T=
NM_001075.6:c.718+575T= MANE Select NP_001066.1:n.718+575T=
NM_001144767.3:c.467-717T= NP_001138239.1:n.467-717T=
NM_001290091.2:c.-26-717T= NP_001277020.1:n.-26-717T=
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