Canonical Allele Identifier: CA12189316
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs9394159

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650385A>T , CM000668.2:g.33650385A>T GRCh38
NC_000006.11:g.33618162A>T , CM000668.1:g.33618162A>T GRCh37
NC_000006.10:g.33726140A>T NCBI36
NG_027729.1:g.34007A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.161-5381A>T MANE Select ENSP00000475177.1:p.=
ENST00000374316.9:c.161-5381A>T ENSP00000363435.4:p.=
ENST00000605930.2:c.161-5381A>T ENSP00000475177.1:p.=
NM_002224.3:c.161-5381A>T NP_002215.2:p.=
XM_011514576.1:c.230-5381A>T XP_011512878.1:p.=
XM_017010832.1:c.161-5381A>T XP_016866321.1:p.=
NM_002224.4:c.161-5381A>T MANE Select NP_002215.2:p.=