Canonical Allele Identifier: CA102010705
Gene: GRID2 HGNC NCBI
COSMIC:
COSN23615897 (not active)
MyVariant.info:
GRCh38 chr4:g.92399876C>T
GRCh37 chr4:g.93321027C>T
gnomAD v2:
4:93321027 C / T
gnomAD v3:
4:92399876 C / T
gnomAD v4:
chr4-92399876-C-T
Joint Max Group AF 0.07456022 (AFR)
Genomes Max Group AF 0.07456022 (AFR)
dbSNP:
7666831
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92399876C>T , CM000666.2:g.92399876C>T GRCh38
NC_000004.11:g.93321027C>T , CM000666.1:g.93321027C>T GRCh37
NC_000004.10:g.93540050C>T NCBI36
NG_034113.1:g.100478C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282020.9:c.88+95132C>T MANE Select ENSP00000282020.4:n.88+95132C>T
ENST00000282020.8:c.88+95132C>T ENSP00000282020.4:n.88+95132C>T
ENST00000505687.5:n.260+95132C>T
ENST00000510992.5:c.88+95132C>T ENSP00000421257.1:n.88+95132C>T
NM_001286838.1:c.88+95132C>T NP_001273767.1:n.88+95132C>T
NM_001510.3:c.88+95132C>T NP_001501.2:n.88+95132C>T
XM_017008122.2:c.88+95132C>T XP_016863611.1:n.88+95132C>T
XM_024454024.1:c.88+95132C>T XP_024309792.1:n.88+95132C>T
NM_001510.4:c.88+95132C>T MANE Select NP_001501.2:n.88+95132C>T
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