Canonical Allele Identifier: CA2023580625
Gene: ITPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.26759722A= , CM000674.2:g.26759722A= GRCh38
NC_000012.11:g.26912655A= , CM000674.1:g.26912655A= GRCh37
NC_000012.10:g.26803922A= NCBI36
NG_042142.1:g.78477T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381340.8:c.163+30435T= MANE Select ENSP00000370744.3:n.163+30435T=
ENST00000242737.5:c.163+30435T= ENSP00000242737.5:n.163+30435T=
ENST00000381340.7:c.163+30435T= ENSP00000370744.3:n.163+30435T=
ENST00000545235.1:c.93-33957T= ENSP00000440548.1:n.93-33957T=
NM_002223.2:c.163+30435T= NP_002214.2:n.163+30435T=
NM_002223.3:c.163+30435T= NP_002214.2:n.163+30435T=
XR_931288.1:n.579+30435T=
XM_017019266.1:c.163+30435T= XP_016874755.1:n.163+30435T=
XM_017019267.1:c.97+30435T= XP_016874756.1:n.97+30435T=
XM_017019269.2:c.163+30435T= XP_016874758.1:n.163+30435T=
XR_001748686.2:n.579+30435T=
XR_001748687.1:n.579+30435T=
NM_002223.4:c.163+30435T= MANE Select NP_002214.2:n.163+30435T=