Canonical Allele Identifier: CA201727216
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs922736156
gnomAD v3: 9-137139100-G-C
gnomAD v4: 9-137139100-G-C
MyVariant Identifiers: chr9:g.140033552G>C (hg19) chr9:g.137139100G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139100G>C , CM000671.2:g.137139100G>C GRCh38
NC_000009.11:g.140033552G>C , CM000671.1:g.140033552G>C GRCh37
NC_000009.10:g.139153373G>C NCBI36
NG_011507.1:g.4944G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-387G>C ENSP00000360615.3:n.-387G>C
ENST00000371561.7:c.-387G>C ENSP00000360616.3:n.-387G>C
XM_005266073.4:c.-387G>C XP_005266130.1:n.-387G>C
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