Canonical Allele Identifier: CA591214845
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1254044187
gnomAD v2: 9-140033566-G-A
gnomAD v3: 9-137139114-G-A
gnomAD v4: 9-137139114-G-A
MyVariant Identifiers: chr9:g.140033566G>A (hg19) chr9:g.137139114G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139114G>A , CM000671.2:g.137139114G>A GRCh38
NC_000009.11:g.140033566G>A , CM000671.1:g.140033566G>A GRCh37
NC_000009.10:g.139153387G>A NCBI36
NG_011507.1:g.4958G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-373G>A ENSP00000360615.3:n.-373G>A
ENST00000371561.7:c.-373G>A ENSP00000360616.3:n.-373G>A
XM_005266073.3:c.-373G>A XP_005266130.1:n.-373G>A
XM_005266073.4:c.-373G>A XP_005266130.1:n.-373G>A
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