Canonical Allele Identifier: CA1620116655
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1582138979
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33668788T>C , CM000668.2:g.33668788T>C GRCh38
NC_000006.11:g.33636565T>C , CM000668.1:g.33636565T>C GRCh37
NC_000006.10:g.33744543T>C NCBI36
NG_027729.1:g.52410T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.2006+154T>C MANE Select ENSP00000475177.1:n.2006+154T>C
ENST00000374316.9:c.2006+154T>C ENSP00000363435.4:n.2006+154T>C
ENST00000605930.2:c.2006+154T>C ENSP00000475177.1:n.2006+154T>C
NM_002224.3:c.2006+154T>C NP_002215.2:n.2006+154T>C
XM_011514576.1:c.2075+154T>C XP_011512878.1:n.2075+154T>C
XM_011514577.1:c.1823+154T>C XP_011512879.1:n.1823+154T>C
XM_011514577.3:c.1823+154T>C XP_011512879.1:n.1823+154T>C
XM_017010832.1:c.2006+154T>C XP_016866321.1:n.2006+154T>C
NM_002224.4:c.2006+154T>C MANE Select NP_002215.2:n.2006+154T>C
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