Canonical Allele Identifier: CA857768729
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1242240749
MyVariant Identifiers: chr9:g.104348020_104348021insC (hg19) chr9:g.101585738_101585739insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585740dup , CM000671.2:g.101585740dup GRCh38
NC_000009.11:g.104348022dup , CM000671.1:g.104348022dup GRCh37
NC_000009.10:g.103387843dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6379dup MANE Select ENSP00000355155.3:n.2767-6379dup
ENST00000361820.3:c.2767-6379dup ENSP00000355155.3:n.2767-6379dup
NM_133445.2:c.2767-6379dup NP_597702.2:n.2767-6379dup
NM_133445.3:c.2767-6379dup MANE Select NP_597702.2:n.2767-6379dup
Search 100 bp 5'
Search 100 bp 3'