Canonical Allele Identifier: CA857763641
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1466733087
MyVariant Identifiers: chr9:g.104378104T>C (hg19) chr9:g.101615822T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615822T>C , CM000671.2:g.101615822T>C GRCh38
NC_000009.11:g.104378104T>C , CM000671.1:g.104378104T>C GRCh37
NC_000009.10:g.103417925T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2295A>G MANE Select ENSP00000355155.3:n.2615-2295A>G
ENST00000361820.3:c.2615-2295A>G ENSP00000355155.3:n.2615-2295A>G
NM_133445.2:c.2615-2295A>G NP_597702.2:n.2615-2295A>G
XM_011518211.1:c.2615-2295A>G XP_011516513.1:n.2615-2295A>G
XM_011518212.1:c.2615-2295A>G XP_011516514.1:n.2615-2295A>G
XR_929711.1:n.2702-2295A>G
XM_011518211.2:c.2615-2295A>G XP_011516513.1:n.2615-2295A>G
NM_133445.3:c.2615-2295A>G MANE Select NP_597702.2:n.2615-2295A>G
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