Canonical Allele Identifier: CA669397464
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1470491526
gnomAD v3: 10-85848729-T-C
gnomAD v4: 10-85848729-T-C
MyVariant Identifiers: chr10:g.87608486T>C (hg19) chr10:g.85848729T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848729T>C , CM000672.2:g.85848729T>C GRCh38
NC_000010.10:g.87608486T>C , CM000672.1:g.87608486T>C GRCh37
NC_000010.9:g.87598466T>C NCBI36
NG_011875.1:g.522765A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.1233+5767A>G MANE Select ENSP00000330148.7:n.1233+5767A>G
ENST00000327946.11:c.1233+5767A>G ENSP00000330148.7:n.1233+5767A>G
ENST00000464741.2:c.1233+5767A>G ENSP00000433064.1:n.1233+5767A>G
ENST00000536331.5:c.453+5767A>G ENSP00000444455.2:n.453+5767A>G
NM_017551.2:c.1233+5767A>G NP_060021.1:n.1233+5767A>G
XM_011539720.1:c.1233+5767A>G XP_011538022.1:n.1233+5767A>G
XM_011539720.2:c.1233+5767A>G XP_011538022.1:n.1233+5767A>G
NM_017551.3:c.1233+5767A>G MANE Select NP_060021.1:n.1233+5767A>G
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