Canonical Allele Identifier: CA197290844
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs187041645
gnomAD v3: 9-101585906-T-A
gnomAD v4: 9-101585906-T-A
MyVariant Identifiers: chr9:g.104348188T>A (hg19) chr9:g.101585906T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585906T>A , CM000671.2:g.101585906T>A GRCh38
NC_000009.11:g.104348188T>A , CM000671.1:g.104348188T>A GRCh37
NC_000009.10:g.103388009T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6546A>T MANE Select ENSP00000355155.3:n.2767-6546A>T
ENST00000361820.3:c.2767-6546A>T ENSP00000355155.3:n.2767-6546A>T
NM_133445.2:c.2767-6546A>T NP_597702.2:n.2767-6546A>T
NM_133445.3:c.2767-6546A>T MANE Select NP_597702.2:n.2767-6546A>T
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