Canonical Allele Identifier: CA201727214
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs910878705
gnomAD v4: 9-137139099-G-A
MyVariant Identifiers: chr9:g.140033551G>A (hg19) chr9:g.137139099G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139099G>A , CM000671.2:g.137139099G>A GRCh38
NC_000009.11:g.140033551G>A , CM000671.1:g.140033551G>A GRCh37
NC_000009.10:g.139153372G>A NCBI36
NG_011507.1:g.4943G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-388G>A ENSP00000360615.3:n.-388G>A
ENST00000371561.7:c.-388G>A ENSP00000360616.3:n.-388G>A
XM_005266073.4:c.-388G>A XP_005266130.1:n.-388G>A
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