Canonical Allele Identifier: CA1127450436
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827948381
gnomAD v3: 9-101586219-T-C
gnomAD v4: 9-101586219-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101586219T>C , CM000671.2:g.101586219T>C GRCh38
NC_000009.11:g.104348501T>C , CM000671.1:g.104348501T>C GRCh37
NC_000009.10:g.103388322T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6859A>G MANE Select ENSP00000355155.3:n.2767-6859A>G
ENST00000361820.3:c.2767-6859A>G ENSP00000355155.3:n.2767-6859A>G
NM_133445.2:c.2767-6859A>G NP_597702.2:n.2767-6859A>G
NM_133445.3:c.2767-6859A>G MANE Select NP_597702.2:n.2767-6859A>G
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