Canonical Allele Identifier: CA1127450318
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827944012
gnomAD v3: 9-101585783-C-A
gnomAD v4: 9-101585783-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585783C>A , CM000671.2:g.101585783C>A GRCh38
NC_000009.11:g.104348065C>A , CM000671.1:g.104348065C>A GRCh37
NC_000009.10:g.103387886C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6423G>T MANE Select ENSP00000355155.3:n.2767-6423G>T
ENST00000361820.3:c.2767-6423G>T ENSP00000355155.3:n.2767-6423G>T
NM_133445.2:c.2767-6423G>T NP_597702.2:n.2767-6423G>T
NM_133445.3:c.2767-6423G>T MANE Select NP_597702.2:n.2767-6423G>T
Search 100 bp 5'
Search 100 bp 3'