Canonical Allele Identifier: CA1465883737
Gene: UGT2B10 HGNC NCBI

Linked Data

dbSNP Id: rs1737237711
gnomAD v4: 4-68816792-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68816792G>A , CM000666.2:g.68816792G>A GRCh38
NC_000004.11:g.69682510G>A , CM000666.1:g.69682510G>A GRCh37
NC_000004.10:g.69717099G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+55G>A MANE Select ENSP00000265403.7:n.718+55G>A
ENST00000265403.11:c.718+55G>A ENSP00000265403.7:n.718+55G>A
ENST00000458688.2:c.466+307G>A ENSP00000413420.2:n.466+307G>A
NM_001075.5:c.718+55G>A NP_001066.1:n.718+55G>A
NM_001144767.2:c.466+307G>A NP_001138239.1:n.466+307G>A
NM_001290091.1:c.-27+620G>A NP_001277020.1:n.-27+620G>A
XM_017008585.2:c.718+55G>A XP_016864074.1:n.718+55G>A
NM_001075.6:c.718+55G>A MANE Select NP_001066.1:n.718+55G>A
NM_001144767.3:c.466+307G>A NP_001138239.1:n.466+307G>A
NM_001290091.2:c.-27+620G>A NP_001277020.1:n.-27+620G>A
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