Canonical Allele Identifier: CA857768817
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1473998623
MyVariant Identifiers: chr9:g.104348194G>T (hg19) chr9:g.101585912G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585912G>T , CM000671.2:g.101585912G>T GRCh38
NC_000009.11:g.104348194G>T , CM000671.1:g.104348194G>T GRCh37
NC_000009.10:g.103388015G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6552C>A MANE Select ENSP00000355155.3:n.2767-6552C>A
ENST00000361820.3:c.2767-6552C>A ENSP00000355155.3:n.2767-6552C>A
NM_133445.2:c.2767-6552C>A NP_597702.2:n.2767-6552C>A
NM_133445.3:c.2767-6552C>A MANE Select NP_597702.2:n.2767-6552C>A
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