Canonical Allele Identifier: CA197290876
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1005644600
gnomAD v2: 9-104348221-T-C
gnomAD v3: 9-101585939-T-C
gnomAD v4: 9-101585939-T-C
MyVariant Identifiers: chr9:g.104348221T>C (hg19) chr9:g.101585939T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585939T>C , CM000671.2:g.101585939T>C GRCh38
NC_000009.11:g.104348221T>C , CM000671.1:g.104348221T>C GRCh37
NC_000009.10:g.103388042T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6579A>G MANE Select ENSP00000355155.3:n.2767-6579A>G
ENST00000361820.3:c.2767-6579A>G ENSP00000355155.3:n.2767-6579A>G
NM_133445.2:c.2767-6579A>G NP_597702.2:n.2767-6579A>G
NM_133445.3:c.2767-6579A>G MANE Select NP_597702.2:n.2767-6579A>G
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