Canonical Allele Identifier: CA1620116651
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1764680671
gnomAD v4: 6-33668786-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33668786C>T , CM000668.2:g.33668786C>T GRCh38
NC_000006.11:g.33636563C>T , CM000668.1:g.33636563C>T GRCh37
NC_000006.10:g.33744541C>T NCBI36
NG_027729.1:g.52408C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2006+152C>T MANE Select ENSP00000475177.1:n.2006+152C>T
ENST00000374316.9:c.2006+152C>T ENSP00000363435.4:n.2006+152C>T
ENST00000605930.2:c.2006+152C>T ENSP00000475177.1:n.2006+152C>T
NM_002224.3:c.2006+152C>T NP_002215.2:n.2006+152C>T
XM_011514576.1:c.2075+152C>T XP_011512878.1:n.2075+152C>T
XM_011514577.1:c.1823+152C>T XP_011512879.1:n.1823+152C>T
XM_011514577.3:c.1823+152C>T XP_011512879.1:n.1823+152C>T
XM_017010832.1:c.2006+152C>T XP_016866321.1:n.2006+152C>T
NM_002224.4:c.2006+152C>T MANE Select NP_002215.2:n.2006+152C>T