Canonical Allele Identifier: CA553362943

Gene: GRID2

Linked Data

• dbSNP Id: rs1051049155
• gnomAD v2: 4-93697102-G-T
• gnomAD v3: 4-92775951-G-T
• gnomAD v4: 4-92775951-G-T
• MyVariant Identifiers: chr4:g.93697102G>T (hg19) ; chr4:g.92775951G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.92775951G>T , CM000666.2:g.92775951G>T	GRCh38
NC_000004.11:g.93697102G>T , CM000666.1:g.93697102G>T	GRCh37
NC_000004.10:g.93916125G>T	NCBI36
NG_034113.1:g.476553G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282020.9:c.244+185665G>T MANE Select	ENSP00000282020.4:n.244+185665G>T
ENST00000282020.8:c.244+185665G>T	ENSP00000282020.4:n.244+185665G>T
ENST00000505687.5:n.416+185665G>T
ENST00000510992.5:c.244+185665G>T	ENSP00000421257.1:n.244+185665G>T
NM_001286838.1:c.244+185665G>T	NP_001273767.1:n.244+185665G>T
NM_001510.3:c.244+185665G>T	NP_001501.2:n.244+185665G>T
XM_017008122.2:c.244+185665G>T	XP_016863611.1:n.244+185665G>T
XM_024454024.1:c.244+185665G>T	XP_024309792.1:n.244+185665G>T
NM_001510.4:c.244+185665G>T MANE Select	NP_001501.2:n.244+185665G>T