Canonical Allele Identifier: CA2943003
Gene: UGT2B10 HGNC NCBI

Linked Data

dbSNP Id: rs769235854
ExAC: 4:69682461 A / AT
gnomAD v2: 4-69682461-A-AT
gnomAD v3: 4-68816743-A-AT
gnomAD v4: 4-68816743-A-AT
MyVariant Identifiers: chr4:g.69682462_69682463insT (hg19) chr4:g.69682461_69682462insT (hg19) chr4:g.68816744_68816745insT (hg38) chr4:g.68816743_68816744insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68816750dup , CM000666.2:g.68816750dup GRCh38
NC_000004.11:g.69682468dup , CM000666.1:g.69682468dup GRCh37
NC_000004.10:g.69717057dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+13dup MANE Select ENSP00000265403.7:n.718+13dup
ENST00000265403.11:c.718+13dup ENSP00000265403.7:n.718+13dup
ENST00000458688.2:c.466+265dup ENSP00000413420.2:n.466+265dup
NM_001075.5:c.718+13dup NP_001066.1:n.718+13dup
NM_001144767.2:c.466+265dup NP_001138239.1:n.466+265dup
NM_001290091.1:c.-27+578dup NP_001277020.1:n.-27+578dup
XM_017008585.2:c.718+13dup XP_016864074.1:n.718+13dup
NM_001075.6:c.718+13dup MANE Select NP_001066.1:n.718+13dup
NM_001144767.3:c.466+265dup NP_001138239.1:n.466+265dup
NM_001290091.2:c.-27+578dup NP_001277020.1:n.-27+578dup
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