Canonical Allele Identifier: CA591214843
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1206576042
gnomAD v2: 9-140033564-G-A
gnomAD v3: 9-137139112-G-A
gnomAD v4: 9-137139112-G-A
MyVariant Identifiers: chr9:g.140033564G>A (hg19) chr9:g.137139112G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139112G>A , CM000671.2:g.137139112G>A GRCh38
NC_000009.11:g.140033564G>A , CM000671.1:g.140033564G>A GRCh37
NC_000009.10:g.139153385G>A NCBI36
NG_011507.1:g.4956G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-375G>A ENSP00000360615.3:n.-375G>A
ENST00000371561.7:c.-375G>A ENSP00000360616.3:n.-375G>A
XM_005266073.3:c.-375G>A XP_005266130.1:n.-375G>A
XM_005266073.4:c.-375G>A XP_005266130.1:n.-375G>A
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