Canonical Allele Identifier: CA201727211
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs983815203
gnomAD v4: 9-137139098-C-A
MyVariant Identifiers: chr9:g.140033550C>A (hg19) chr9:g.137139098C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139098C>A , CM000671.2:g.137139098C>A GRCh38
NC_000009.11:g.140033550C>A , CM000671.1:g.140033550C>A GRCh37
NC_000009.10:g.139153371C>A NCBI36
NG_011507.1:g.4942C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-389C>A ENSP00000360615.3:n.-389C>A
ENST00000371561.7:c.-389C>A ENSP00000360616.3:n.-389C>A
XM_005266073.4:c.-389C>A XP_005266130.1:n.-389C>A
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