Canonical Allele Identifier: CA797773042

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1385146235
• gnomAD v3: 4-68817230-C-T
• gnomAD v4: 4-68817230-C-T
• MyVariant Identifiers: chr4:g.69682948C>T (hg19) ; chr4:g.68817230C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817230C>T , CM000666.2:g.68817230C>T	GRCh38
NC_000004.11:g.69682948C>T , CM000666.1:g.69682948C>T	GRCh37
NC_000004.10:g.69717537C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+493C>T MANE Select	ENSP00000265403.7:n.718+493C>T
ENST00000265403.11:c.718+493C>T	ENSP00000265403.7:n.718+493C>T
ENST00000458688.2:c.466+745C>T	ENSP00000413420.2:n.466+745C>T
NM_001075.5:c.718+493C>T	NP_001066.1:n.718+493C>T
NM_001144767.2:c.466+745C>T	NP_001138239.1:n.466+745C>T
NM_001290091.1:c.-26-799C>T	NP_001277020.1:n.-26-799C>T
XM_017008585.2:c.718+493C>T	XP_016864074.1:n.718+493C>T
NM_001075.6:c.718+493C>T MANE Select	NP_001066.1:n.718+493C>T
NM_001144767.3:c.466+745C>T	NP_001138239.1:n.466+745C>T
NM_001290091.2:c.-26-799C>T	NP_001277020.1:n.-26-799C>T