Canonical Allele Identifier: CA197290801
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs924700820
MyVariant Identifiers: chr9:g.104348063A>C (hg19) chr9:g.101585781A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585781A>C , CM000671.2:g.101585781A>C GRCh38
NC_000009.11:g.104348063A>C , CM000671.1:g.104348063A>C GRCh37
NC_000009.10:g.103387884A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6421T>G MANE Select ENSP00000355155.3:n.2767-6421T>G
ENST00000361820.3:c.2767-6421T>G ENSP00000355155.3:n.2767-6421T>G
NM_133445.2:c.2767-6421T>G NP_597702.2:n.2767-6421T>G
NM_133445.3:c.2767-6421T>G MANE Select NP_597702.2:n.2767-6421T>G
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