Canonical Allele Identifier: CA1868339572
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1760745327

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585884C>T , CM000671.2:g.101585884C>T GRCh38
NC_000009.11:g.104348166C>T , CM000671.1:g.104348166C>T GRCh37
NC_000009.10:g.103387987C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6524G>A MANE Select ENSP00000355155.3:n.2767-6524G>A
ENST00000361820.3:c.2767-6524G>A ENSP00000355155.3:n.2767-6524G>A
NM_133445.2:c.2767-6524G>A NP_597702.2:n.2767-6524G>A
NM_133445.3:c.2767-6524G>A MANE Select NP_597702.2:n.2767-6524G>A