Canonical Allele Identifier: CA102057967

Gene: GRID2

Linked Data

• dbSNP Id: rs975086972
• gnomAD v2: 4-93697079-T-C
• gnomAD v3: 4-92775928-T-C
• gnomAD v4: 4-92775928-T-C
• MyVariant Identifiers: chr4:g.93697079T>C (hg19) ; chr4:g.92775928T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775928T>C , CM000666.2:g.92775928T>C	GRCh38
NC_000004.11:g.93697079T>C , CM000666.1:g.93697079T>C	GRCh37
NC_000004.10:g.93916102T>C	NCBI36
NG_034113.1:g.476530T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185642T>C MANE Select	ENSP00000282020.4:n.244+185642T>C
ENST00000282020.8:c.244+185642T>C	ENSP00000282020.4:n.244+185642T>C
ENST00000505687.5:n.416+185642T>C
ENST00000510992.5:c.244+185642T>C	ENSP00000421257.1:n.244+185642T>C
NM_001286838.1:c.244+185642T>C	NP_001273767.1:n.244+185642T>C
NM_001510.3:c.244+185642T>C	NP_001501.2:n.244+185642T>C
XM_017008122.2:c.244+185642T>C	XP_016863611.1:n.244+185642T>C
XM_024454024.1:c.244+185642T>C	XP_024309792.1:n.244+185642T>C
NM_001510.4:c.244+185642T>C MANE Select	NP_001501.2:n.244+185642T>C