Canonical Allele Identifier: CA1465883777
Gene: UGT2B10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68816869G= , CM000666.2:g.68816869G= GRCh38
NC_000004.11:g.69682587G= , CM000666.1:g.69682587G= GRCh37
NC_000004.10:g.69717176G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+132G= MANE Select ENSP00000265403.7:n.718+132G=
ENST00000265403.11:c.718+132G= ENSP00000265403.7:n.718+132G=
ENST00000458688.2:c.466+384G= ENSP00000413420.2:n.466+384G=
NM_001075.5:c.718+132G= NP_001066.1:n.718+132G=
NM_001144767.2:c.466+384G= NP_001138239.1:n.466+384G=
NM_001290091.1:c.-27+697G= NP_001277020.1:n.-27+697G=
XM_017008585.2:c.718+132G= XP_016864074.1:n.718+132G=
NM_001075.6:c.718+132G= MANE Select NP_001066.1:n.718+132G=
NM_001144767.3:c.466+384G= NP_001138239.1:n.466+384G=
NM_001290091.2:c.-27+697G= NP_001277020.1:n.-27+697G=
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