Canonical Allele Identifier: CA669432495
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1375126004
gnomAD v3: 10-86124297-G-C
gnomAD v4: 10-86124297-G-C
MyVariant Identifiers: chr10:g.87884054G>C (hg19) chr10:g.86124297G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124297G>C , CM000672.2:g.86124297G>C GRCh38
NC_000010.10:g.87884054G>C , CM000672.1:g.87884054G>C GRCh37
NC_000010.9:g.87874034G>C NCBI36
NG_011875.1:g.247197C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14522C>G MANE Select ENSP00000330148.7:n.726+14522C>G
ENST00000327946.11:c.726+14522C>G ENSP00000330148.7:n.726+14522C>G
ENST00000464741.2:c.726+14522C>G ENSP00000433064.1:n.726+14522C>G
NM_017551.2:c.726+14522C>G NP_060021.1:n.726+14522C>G
XM_011539720.1:c.726+14522C>G XP_011538022.1:n.726+14522C>G
XM_011539720.2:c.726+14522C>G XP_011538022.1:n.726+14522C>G
NM_017551.3:c.726+14522C>G MANE Select NP_060021.1:n.726+14522C>G
Search 100 bp 5'
Search 100 bp 3'