Canonical Allele Identifier: CA197290815
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs559126141
gnomAD v3: 9-101585814-G-T
gnomAD v4: 9-101585814-G-T
MyVariant Identifiers: chr9:g.104348096G>T (hg19) chr9:g.101585814G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585814G>T , CM000671.2:g.101585814G>T GRCh38
NC_000009.11:g.104348096G>T , CM000671.1:g.104348096G>T GRCh37
NC_000009.10:g.103387917G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6454C>A MANE Select ENSP00000355155.3:n.2767-6454C>A
ENST00000361820.3:c.2767-6454C>A ENSP00000355155.3:n.2767-6454C>A
NM_133445.2:c.2767-6454C>A NP_597702.2:n.2767-6454C>A
NM_133445.3:c.2767-6454C>A MANE Select NP_597702.2:n.2767-6454C>A
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