Canonical Allele Identifier: CA800067182

Gene: GRID2

Linked Data

• dbSNP Id: rs1455750252
• gnomAD v3: 4-92775921-C-A
• gnomAD v4: 4-92775921-C-A
• MyVariant Identifiers: chr4:g.93697072C>A (hg19) ; chr4:g.92775921C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775921C>A , CM000666.2:g.92775921C>A	GRCh38
NC_000004.11:g.93697072C>A , CM000666.1:g.93697072C>A	GRCh37
NC_000004.10:g.93916095C>A	NCBI36
NG_034113.1:g.476523C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185635C>A MANE Select	ENSP00000282020.4:n.244+185635C>A
ENST00000282020.8:c.244+185635C>A	ENSP00000282020.4:n.244+185635C>A
ENST00000505687.5:n.416+185635C>A
ENST00000510992.5:c.244+185635C>A	ENSP00000421257.1:n.244+185635C>A
NM_001286838.1:c.244+185635C>A	NP_001273767.1:n.244+185635C>A
NM_001510.3:c.244+185635C>A	NP_001501.2:n.244+185635C>A
XM_017008122.2:c.244+185635C>A	XP_016863611.1:n.244+185635C>A
XM_024454024.1:c.244+185635C>A	XP_024309792.1:n.244+185635C>A
NM_001510.4:c.244+185635C>A MANE Select	NP_001501.2:n.244+185635C>A