Canonical Allele Identifier: CA363697800
Gene: ITPR3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.33636823G>A (hg19) chr6:g.33669046G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33669046G>A , CM000668.2:g.33669046G>A GRCh38
NC_000006.11:g.33636823G>A , CM000668.1:g.33636823G>A GRCh37
NC_000006.10:g.33744801G>A NCBI36
NG_027729.1:g.52668G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2079G>A MANE Select ENSP00000475177.1:p.Trp693Ter
ENST00000374316.9:c.2079G>A ENSP00000363435.4:p.Trp693Ter
ENST00000605930.2:c.2079G>A ENSP00000475177.1:p.Trp693Ter
NM_002224.3:c.2079G>A NP_002215.2:p.Trp693Ter
XM_011514576.1:c.2148G>A XP_011512878.1:p.Trp716Ter
XM_011514577.1:c.1896G>A XP_011512879.1:p.Trp632Ter
XM_011514577.3:c.1896G>A XP_011512879.1:p.Trp632Ter
XM_017010832.1:c.2079G>A XP_016866321.1:p.Trp693Ter
NM_002224.4:c.2079G>A MANE Select NP_002215.2:p.Trp693Ter
Search 100 bp 5'
Search 100 bp 3'