Canonical Allele Identifier: CA552612283

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1261296406
• gnomAD v2: 4-69682463-T-A
• gnomAD v3: 4-68816745-T-A
• gnomAD v4: 4-68816745-T-A
• MyVariant Identifiers: chr4:g.69682463T>A (hg19) ; chr4:g.68816745T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816745T>A , CM000666.2:g.68816745T>A	GRCh38
NC_000004.11:g.69682463T>A , CM000666.1:g.69682463T>A	GRCh37
NC_000004.10:g.69717052T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+8T>A MANE Select	ENSP00000265403.7:n.718+8T>A
ENST00000265403.11:c.718+8T>A	ENSP00000265403.7:n.718+8T>A
ENST00000458688.2:c.466+260T>A	ENSP00000413420.2:n.466+260T>A
NM_001075.5:c.718+8T>A	NP_001066.1:n.718+8T>A
NM_001144767.2:c.466+260T>A	NP_001138239.1:n.466+260T>A
NM_001290091.1:c.-27+573T>A	NP_001277020.1:n.-27+573T>A
XM_017008585.2:c.718+8T>A	XP_016864074.1:n.718+8T>A
NM_001075.6:c.718+8T>A MANE Select	NP_001066.1:n.718+8T>A
NM_001144767.3:c.466+260T>A	NP_001138239.1:n.466+260T>A
NM_001290091.2:c.-27+573T>A	NP_001277020.1:n.-27+573T>A