Canonical Allele Identifier: CA1087691697
Gene: ITPR3 HGNC NCBI

Linked Data

gnomAD v3: 6-33650284-C-A
gnomAD v4: 6-33650284-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650284C>A , CM000668.2:g.33650284C>A GRCh38
NC_000006.11:g.33618061C>A , CM000668.1:g.33618061C>A GRCh37
NC_000006.10:g.33726039C>A NCBI36
NG_027729.1:g.33906C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.161-5482C>A MANE Select ENSP00000475177.1:n.161-5482C>A
ENST00000374316.9:c.161-5482C>A ENSP00000363435.4:n.161-5482C>A
ENST00000605930.2:c.161-5482C>A ENSP00000475177.1:n.161-5482C>A
NM_002224.3:c.161-5482C>A NP_002215.2:n.161-5482C>A
XM_011514576.1:c.230-5482C>A XP_011512878.1:n.230-5482C>A
XM_017010832.1:c.161-5482C>A XP_016866321.1:n.161-5482C>A
NM_002224.4:c.161-5482C>A MANE Select NP_002215.2:n.161-5482C>A
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