Canonical Allele Identifier: CA2023454842

Gene: ITPR2

Linked Data

• dbSNP Id: rs10771283

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.26434645G>T , CM000674.2:g.26434645G>T	GRCh38
NC_000012.11:g.26587578G>T , CM000674.1:g.26587578G>T	GRCh37
NC_000012.10:g.26478845G>T	NCBI36
NG_042142.1:g.403554C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381340.8:c.6769+1576C>A MANE Select	ENSP00000370744.3:n.6769+1576C>A
ENST00000381340.7:c.6769+1576C>A	ENSP00000370744.3:n.6769+1576C>A
ENST00000451599.6:c.1597+1576C>A	ENSP00000408287.2:n.1597+1576C>A
NM_002223.2:c.6769+1576C>A	NP_002214.2:n.6769+1576C>A
NM_002223.3:c.6769+1576C>A	NP_002214.2:n.6769+1576C>A
XM_011520645.1:c.6217+1576C>A	XP_011518947.1:n.6217+1576C>A
XM_011520646.1:c.5836+1576C>A	XP_011518948.1:n.5836+1576C>A
XM_017019266.1:c.6829+1576C>A	XP_016874755.1:n.6829+1576C>A
XM_017019267.1:c.6763+1576C>A	XP_016874756.1:n.6763+1576C>A
XR_001748686.2:n.7245+1576C>A
NM_002223.4:c.6769+1576C>A MANE Select	NP_002214.2:n.6769+1576C>A