Canonical Allele Identifier: CA1087691702
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1764158599
gnomAD v3: 6-33650366-A-G
gnomAD v4: 6-33650366-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650366A>G , CM000668.2:g.33650366A>G GRCh38
NC_000006.11:g.33618143A>G , CM000668.1:g.33618143A>G GRCh37
NC_000006.10:g.33726121A>G NCBI36
NG_027729.1:g.33988A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.161-5400A>G MANE Select ENSP00000475177.1:n.161-5400A>G
ENST00000374316.9:c.161-5400A>G ENSP00000363435.4:n.161-5400A>G
ENST00000605930.2:c.161-5400A>G ENSP00000475177.1:n.161-5400A>G
NM_002224.3:c.161-5400A>G NP_002215.2:n.161-5400A>G
XM_011514576.1:c.230-5400A>G XP_011512878.1:n.230-5400A>G
XM_017010832.1:c.161-5400A>G XP_016866321.1:n.161-5400A>G
NM_002224.4:c.161-5400A>G MANE Select NP_002215.2:n.161-5400A>G