Canonical Allele Identifier: CA1868339575
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827944924

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585885C>A , CM000671.2:g.101585885C>A GRCh38
NC_000009.11:g.104348167C>A , CM000671.1:g.104348167C>A GRCh37
NC_000009.10:g.103387988C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6525G>T MANE Select ENSP00000355155.3:n.2767-6525G>T
ENST00000361820.3:c.2767-6525G>T ENSP00000355155.3:n.2767-6525G>T
NM_133445.2:c.2767-6525G>T NP_597702.2:n.2767-6525G>T
NM_133445.3:c.2767-6525G>T MANE Select NP_597702.2:n.2767-6525G>T