Canonical Allele Identifier: CA2943016

Gene: UGT2B10

Linked Data

• dbSNP Id: rs751616184
• ExAC: 4:69682495 A / C
• gnomAD v2: 4-69682495-A-C
• gnomAD v3: 4-68816777-A-C
• gnomAD v4: 4-68816777-A-C
• MyVariant Identifiers: chr4:g.69682495A>C (hg19) ; chr4:g.68816777A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816777A>C , CM000666.2:g.68816777A>C	GRCh38
NC_000004.11:g.69682495A>C , CM000666.1:g.69682495A>C	GRCh37
NC_000004.10:g.69717084A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+40A>C MANE Select	ENSP00000265403.7:n.718+40A>C
ENST00000265403.11:c.718+40A>C	ENSP00000265403.7:n.718+40A>C
ENST00000458688.2:c.466+292A>C	ENSP00000413420.2:n.466+292A>C
NM_001075.5:c.718+40A>C	NP_001066.1:n.718+40A>C
NM_001144767.2:c.466+292A>C	NP_001138239.1:n.466+292A>C
NM_001290091.1:c.-27+605A>C	NP_001277020.1:n.-27+605A>C
XM_017008585.2:c.718+40A>C	XP_016864074.1:n.718+40A>C
NM_001075.6:c.718+40A>C MANE Select	NP_001066.1:n.718+40A>C
NM_001144767.3:c.466+292A>C	NP_001138239.1:n.466+292A>C
NM_001290091.2:c.-27+605A>C	NP_001277020.1:n.-27+605A>C