Canonical Allele Identifier: CA669397406
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1346052738
gnomAD v3: 10-85848626-A-G
gnomAD v4: 10-85848626-A-G
MyVariant Identifiers: chr10:g.87608383A>G (hg19) chr10:g.85848626A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848626A>G , CM000672.2:g.85848626A>G GRCh38
NC_000010.10:g.87608383A>G , CM000672.1:g.87608383A>G GRCh37
NC_000010.9:g.87598363A>G NCBI36
NG_011875.1:g.522868T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.1233+5870T>C MANE Select ENSP00000330148.7:n.1233+5870T>C
ENST00000327946.11:c.1233+5870T>C ENSP00000330148.7:n.1233+5870T>C
ENST00000464741.2:c.1233+5870T>C ENSP00000433064.1:n.1233+5870T>C
ENST00000536331.5:c.453+5870T>C ENSP00000444455.2:n.453+5870T>C
NM_017551.2:c.1233+5870T>C NP_060021.1:n.1233+5870T>C
XM_011539720.1:c.1233+5870T>C XP_011538022.1:n.1233+5870T>C
XM_011539720.2:c.1233+5870T>C XP_011538022.1:n.1233+5870T>C
NM_017551.3:c.1233+5870T>C MANE Select NP_060021.1:n.1233+5870T>C
Search 100 bp 5'
Search 100 bp 3'