Canonical Allele Identifier: CA363698130

Gene: ITPR3

Linked Data

• gnomAD v4: 6-33669119-G-C
• MyVariant Identifiers: chr6:g.33636896G>C (hg19) ; chr6:g.33669119G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33669119G>C , CM000668.2:g.33669119G>C	GRCh38
NC_000006.11:g.33636896G>C , CM000668.1:g.33636896G>C	GRCh37
NC_000006.10:g.33744874G>C	NCBI36
NG_027729.1:g.52741G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000605930.3:c.2152G>C MANE Select	ENSP00000475177.1:p.Gly718Arg
ENST00000374316.9:c.2152G>C	ENSP00000363435.4:p.Gly718Arg
ENST00000605930.2:c.2152G>C	ENSP00000475177.1:p.Gly718Arg
NM_002224.3:c.2152G>C	NP_002215.2:p.Gly718Arg
XM_011514576.1:c.2221G>C	XP_011512878.1:p.Gly741Arg
XM_011514577.1:c.1969G>C	XP_011512879.1:p.Gly657Arg
XM_011514577.3:c.1969G>C	XP_011512879.1:p.Gly657Arg
XM_017010832.1:c.2152G>C	XP_016866321.1:p.Gly718Arg
NM_002224.4:c.2152G>C MANE Select	NP_002215.2:p.Gly718Arg