Canonical Allele Identifier: CA1868339535
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827944267
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585808del , CM000671.2:g.101585808del GRCh38
NC_000009.11:g.104348090del , CM000671.1:g.104348090del GRCh37
NC_000009.10:g.103387911del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6448del MANE Select ENSP00000355155.3:n.2767-6448del
ENST00000361820.3:c.2767-6448del ENSP00000355155.3:n.2767-6448del
NM_133445.2:c.2767-6448del NP_597702.2:n.2767-6448del
NM_133445.3:c.2767-6448del MANE Select NP_597702.2:n.2767-6448del
Search 100 bp 5'
Search 100 bp 3'