Canonical Allele Identifier: CA857763600
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1170851525
MyVariant Identifiers: chr9:g.104378019G>T (hg19) chr9:g.101615737G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101615737G>T , CM000671.2:g.101615737G>T GRCh38
NC_000009.11:g.104378019G>T , CM000671.1:g.104378019G>T GRCh37
NC_000009.10:g.103417840G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2615-2210C>A MANE Select ENSP00000355155.3:n.2615-2210C>A
ENST00000361820.3:c.2615-2210C>A ENSP00000355155.3:n.2615-2210C>A
NM_133445.2:c.2615-2210C>A NP_597702.2:n.2615-2210C>A
XM_011518211.1:c.2615-2210C>A XP_011516513.1:n.2615-2210C>A
XM_011518212.1:c.2615-2210C>A XP_011516514.1:n.2615-2210C>A
XR_929711.1:n.2702-2210C>A
XM_011518211.2:c.2615-2210C>A XP_011516513.1:n.2615-2210C>A
NM_133445.3:c.2615-2210C>A MANE Select NP_597702.2:n.2615-2210C>A
Search 100 bp 5'
Search 100 bp 3'