Canonical Allele Identifier: CA201727221
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1047094674
gnomAD v3: 9-137139130-C-T
gnomAD v4: 9-137139130-C-T
MyVariant Identifiers: chr9:g.140033582C>T (hg19) chr9:g.137139130C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139130C>T , CM000671.2:g.137139130C>T GRCh38
NC_000009.11:g.140033582C>T , CM000671.1:g.140033582C>T GRCh37
NC_000009.10:g.139153403C>T NCBI36
NG_011507.1:g.4974C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-357C>T ENSP00000360615.3:n.-357C>T
ENST00000371561.7:c.-357C>T ENSP00000360616.3:n.-357C>T
XM_005266073.3:c.-357C>T XP_005266130.1:n.-357C>T
XM_005266073.4:c.-357C>T XP_005266130.1:n.-357C>T
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