Canonical Allele Identifier: CA363698136
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1764690668

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33669120G>A , CM000668.2:g.33669120G>A GRCh38
NC_000006.11:g.33636897G>A , CM000668.1:g.33636897G>A GRCh37
NC_000006.10:g.33744875G>A NCBI36
NG_027729.1:g.52742G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000605930.3:c.2153G>A MANE Select ENSP00000475177.1:p.Gly718Asp
ENST00000374316.9:c.2153G>A ENSP00000363435.4:p.Gly718Asp
ENST00000605930.2:c.2153G>A ENSP00000475177.1:p.Gly718Asp
NM_002224.3:c.2153G>A NP_002215.2:p.Gly718Asp
XM_011514576.1:c.2222G>A XP_011512878.1:p.Gly741Asp
XM_011514577.1:c.1970G>A XP_011512879.1:p.Gly657Asp
XM_011514577.3:c.1970G>A XP_011512879.1:p.Gly657Asp
XM_017010832.1:c.2153G>A XP_016866321.1:p.Gly718Asp
NM_002224.4:c.2153G>A MANE Select NP_002215.2:p.Gly718Asp