Canonical Allele Identifier: CA210671042
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1047094344
gnomAD v3: 10-86124412-A-T
gnomAD v4: 10-86124412-A-T
MyVariant Identifiers: chr10:g.87884169A>T (hg19) chr10:g.86124412A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86124412A>T , CM000672.2:g.86124412A>T GRCh38
NC_000010.10:g.87884169A>T , CM000672.1:g.87884169A>T GRCh37
NC_000010.9:g.87874149A>T NCBI36
NG_011875.1:g.247082T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.726+14407T>A MANE Select ENSP00000330148.7:n.726+14407T>A
ENST00000327946.11:c.726+14407T>A ENSP00000330148.7:n.726+14407T>A
ENST00000464741.2:c.726+14407T>A ENSP00000433064.1:n.726+14407T>A
NM_017551.2:c.726+14407T>A NP_060021.1:n.726+14407T>A
XM_011539720.1:c.726+14407T>A XP_011538022.1:n.726+14407T>A
XM_011539720.2:c.726+14407T>A XP_011538022.1:n.726+14407T>A
NM_017551.3:c.726+14407T>A MANE Select NP_060021.1:n.726+14407T>A
Search 100 bp 5'
Search 100 bp 3'