Canonical Allele Identifier: CA1868339563
Community Standard Title: NM_133445.3(GRIN3A):c.2767-6508C=
Gene: GRIN3A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585868G= , CM000671.2:g.101585868G= GRCh38
NC_000009.11:g.104348150G= , CM000671.1:g.104348150G= GRCh37
NC_000009.10:g.103387971G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_133445.3:c.2767-6508C= MANE Select NP_597702.2:n.2767-6508C=
ENST00000361820.6:c.2767-6508C= MANE Select ENSP00000355155.3:n.2767-6508C=
NM_133445.2:c.2767-6508C= NP_597702.2:n.2767-6508C=
ENST00000361820.3:c.2767-6508C= ENSP00000355155.3:n.2767-6508C=
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