Canonical Allele Identifier: CA1465884061
Gene: UGT2B10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68817309A= , CM000666.2:g.68817309A= GRCh38
NC_000004.11:g.69683027A= , CM000666.1:g.69683027A= GRCh37
NC_000004.10:g.69717616A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+572A= MANE Select ENSP00000265403.7:n.718+572A=
ENST00000265403.11:c.718+572A= ENSP00000265403.7:n.718+572A=
ENST00000458688.2:c.467-720A= ENSP00000413420.2:n.467-720A=
NM_001075.5:c.718+572A= NP_001066.1:n.718+572A=
NM_001144767.2:c.467-720A= NP_001138239.1:n.467-720A=
NM_001290091.1:c.-26-720A= NP_001277020.1:n.-26-720A=
XM_017008585.2:c.718+572A= XP_016864074.1:n.718+572A=
NM_001075.6:c.718+572A= MANE Select NP_001066.1:n.718+572A=
NM_001144767.3:c.467-720A= NP_001138239.1:n.467-720A=
NM_001290091.2:c.-26-720A= NP_001277020.1:n.-26-720A=
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