Canonical Allele Identifier: CA857768725
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1166200775
MyVariant Identifiers: chr9:g.104348001C>G (hg19) chr9:g.101585719C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585719C>G , CM000671.2:g.101585719C>G GRCh38
NC_000009.11:g.104348001C>G , CM000671.1:g.104348001C>G GRCh37
NC_000009.10:g.103387822C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6359G>C MANE Select ENSP00000355155.3:n.2767-6359G>C
ENST00000361820.3:c.2767-6359G>C ENSP00000355155.3:n.2767-6359G>C
NM_133445.2:c.2767-6359G>C NP_597702.2:n.2767-6359G>C
NM_133445.3:c.2767-6359G>C MANE Select NP_597702.2:n.2767-6359G>C
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