Canonical Allele Identifier: CA797772796

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1459828002
• gnomAD v4: 4-68816809-CCATAAAGT-C
• MyVariant Identifiers: chr4:g.69682528_69682535del (hg19) ; chr4:g.68816810_68816817del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816812_68816819del , CM000666.2:g.68816812_68816819del	GRCh38
NC_000004.11:g.69682530_69682537del , CM000666.1:g.69682530_69682537del	GRCh37
NC_000004.10:g.69717119_69717126del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+75_718+82del MANE Select	ENSP00000265403.7:n.718+75_718+82del
ENST00000265403.11:c.718+75_718+82del	ENSP00000265403.7:n.718+75_718+82del
ENST00000458688.2:c.466+327_466+334del	ENSP00000413420.2:n.466+327_466+334del
NM_001075.5:c.718+75_718+82del	NP_001066.1:n.718+75_718+82del
NM_001144767.2:c.466+327_466+334del	NP_001138239.1:n.466+327_466+334del
NM_001290091.1:c.-27+640_-27+647del	NP_001277020.1:n.-27+640_-27+647del
XM_017008585.2:c.718+75_718+82del	XP_016864074.1:n.718+75_718+82del
NM_001075.6:c.718+75_718+82del MANE Select	NP_001066.1:n.718+75_718+82del
NM_001144767.3:c.466+327_466+334del	NP_001138239.1:n.466+327_466+334del
NM_001290091.2:c.-27+640_-27+647del	NP_001277020.1:n.-27+640_-27+647del