Canonical Allele Identifier: CA1868339603
Gene: GRIN3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585950G= , CM000671.2:g.101585950G= GRCh38
NC_000009.11:g.104348232G= , CM000671.1:g.104348232G= GRCh37
NC_000009.10:g.103388053G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6590C= MANE Select ENSP00000355155.3:n.2767-6590C=
ENST00000361820.3:c.2767-6590C= ENSP00000355155.3:n.2767-6590C=
NM_133445.2:c.2767-6590C= NP_597702.2:n.2767-6590C=
NM_133445.3:c.2767-6590C= MANE Select NP_597702.2:n.2767-6590C=
Search 100 bp 5'
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