Canonical Allele Identifier: CA1063776603

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1737239667
• gnomAD v3: 4-68816856-GA-G
• gnomAD v4: 4-68816856-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816860del , CM000666.2:g.68816860del	GRCh38
NC_000004.11:g.69682578del , CM000666.1:g.69682578del	GRCh37
NC_000004.10:g.69717167del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+123del MANE Select	ENSP00000265403.7:n.718+123del
ENST00000265403.11:c.718+123del	ENSP00000265403.7:n.718+123del
ENST00000458688.2:c.466+375del	ENSP00000413420.2:n.466+375del
NM_001075.5:c.718+123del	NP_001066.1:n.718+123del
NM_001144767.2:c.466+375del	NP_001138239.1:n.466+375del
NM_001290091.1:c.-27+688del	NP_001277020.1:n.-27+688del
XM_017008585.2:c.718+123del	XP_016864074.1:n.718+123del
NM_001075.6:c.718+123del MANE Select	NP_001066.1:n.718+123del
NM_001144767.3:c.466+375del	NP_001138239.1:n.466+375del
NM_001290091.2:c.-27+688del	NP_001277020.1:n.-27+688del