Canonical Allele Identifier: CA669397460
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1399595082
gnomAD v3: 10-85848725-G-T
gnomAD v4: 10-85848725-G-T
MyVariant Identifiers: chr10:g.87608482G>T (hg19) chr10:g.85848725G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85848725G>T , CM000672.2:g.85848725G>T GRCh38
NC_000010.10:g.87608482G>T , CM000672.1:g.87608482G>T GRCh37
NC_000010.9:g.87598462G>T NCBI36
NG_011875.1:g.522769C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.1233+5771C>A MANE Select ENSP00000330148.7:n.1233+5771C>A
ENST00000327946.11:c.1233+5771C>A ENSP00000330148.7:n.1233+5771C>A
ENST00000464741.2:c.1233+5771C>A ENSP00000433064.1:n.1233+5771C>A
ENST00000536331.5:c.453+5771C>A ENSP00000444455.2:n.453+5771C>A
NM_017551.2:c.1233+5771C>A NP_060021.1:n.1233+5771C>A
XM_011539720.1:c.1233+5771C>A XP_011538022.1:n.1233+5771C>A
XM_011539720.2:c.1233+5771C>A XP_011538022.1:n.1233+5771C>A
NM_017551.3:c.1233+5771C>A MANE Select NP_060021.1:n.1233+5771C>A
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