Canonical Allele Identifier: CA800067197

Gene: GRID2

Linked Data

• dbSNP Id: rs1484859742
• gnomAD v3: 4-92775934-C-G
• gnomAD v4: 4-92775934-C-G
• MyVariant Identifiers: chr4:g.93697085C>G (hg19) ; chr4:g.92775934C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775934C>G , CM000666.2:g.92775934C>G	GRCh38
NC_000004.11:g.93697085C>G , CM000666.1:g.93697085C>G	GRCh37
NC_000004.10:g.93916108C>G	NCBI36
NG_034113.1:g.476536C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185648C>G MANE Select	ENSP00000282020.4:n.244+185648C>G
ENST00000282020.8:c.244+185648C>G	ENSP00000282020.4:n.244+185648C>G
ENST00000505687.5:n.416+185648C>G
ENST00000510992.5:c.244+185648C>G	ENSP00000421257.1:n.244+185648C>G
NM_001286838.1:c.244+185648C>G	NP_001273767.1:n.244+185648C>G
NM_001510.3:c.244+185648C>G	NP_001501.2:n.244+185648C>G
XM_017008122.2:c.244+185648C>G	XP_016863611.1:n.244+185648C>G
XM_024454024.1:c.244+185648C>G	XP_024309792.1:n.244+185648C>G
NM_001510.4:c.244+185648C>G MANE Select	NP_001501.2:n.244+185648C>G