Canonical Allele Identifier: CA197290747
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs373966718
gnomAD v2: 9-104347967-C-CA
gnomAD v3: 9-101585685-C-CA
gnomAD v4: 9-101585685-C-CA
MyVariant Identifiers: chr9:g.104347967_104347968insA (hg19) chr9:g.101585685_101585686insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585687dup , CM000671.2:g.101585687dup GRCh38
NC_000009.11:g.104347969dup , CM000671.1:g.104347969dup GRCh37
NC_000009.10:g.103387790dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6326dup MANE Select ENSP00000355155.3:n.2767-6326dup
ENST00000361820.3:c.2767-6326dup ENSP00000355155.3:n.2767-6326dup
NM_133445.2:c.2767-6326dup NP_597702.2:n.2767-6326dup
NM_133445.3:c.2767-6326dup MANE Select NP_597702.2:n.2767-6326dup
Search 100 bp 5'
Search 100 bp 3'