Canonical Allele Identifier: CA102057968

Gene: GRID2

Linked Data

• dbSNP Id: rs748582855
• MyVariant Identifiers: chr4:g.93697081C>T (hg19) ; chr4:g.92775930C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775930C>T , CM000666.2:g.92775930C>T	GRCh38
NC_000004.11:g.93697081C>T , CM000666.1:g.93697081C>T	GRCh37
NC_000004.10:g.93916104C>T	NCBI36
NG_034113.1:g.476532C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185644C>T MANE Select	ENSP00000282020.4:n.244+185644C>T
ENST00000282020.8:c.244+185644C>T	ENSP00000282020.4:n.244+185644C>T
ENST00000505687.5:n.416+185644C>T
ENST00000510992.5:c.244+185644C>T	ENSP00000421257.1:n.244+185644C>T
NM_001286838.1:c.244+185644C>T	NP_001273767.1:n.244+185644C>T
NM_001510.3:c.244+185644C>T	NP_001501.2:n.244+185644C>T
XM_017008122.2:c.244+185644C>T	XP_016863611.1:n.244+185644C>T
XM_024454024.1:c.244+185644C>T	XP_024309792.1:n.244+185644C>T
NM_001510.4:c.244+185644C>T MANE Select	NP_001501.2:n.244+185644C>T