Canonical Allele Identifier: CA13004654
Gene: GRIN1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.137138632G>C
GRCh37 chr9:g.140033084G>C
gnomAD v2:
9:140033084 G / C
gnomAD v3:
9:137138632 G / C
gnomAD v4:
chr9-137138632-G-C
Joint Max Group AF 0.17654836 (EAS)
Genomes Max Group AF 0.17159787 (EAS)
Exomes Max Group AF 0.20307758 (EAS)
dbSNP:
11146020
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137138632G>C , CM000671.2:g.137138632G>C GRCh38
NC_000009.11:g.140033084G>C , CM000671.1:g.140033084G>C GRCh37
NC_000009.10:g.139152905G>C NCBI36
NG_011507.1:g.4476G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-855G>C ENSP00000360615.3:n.-855G>C
ENST00000371561.7:c.-855G>C ENSP00000360616.3:n.-855G>C
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