Canonical Allele Identifier: CA15619796
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs11788456

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585868G>A , CM000671.2:g.101585868G>A GRCh38
NC_000009.11:g.104348150G>A , CM000671.1:g.104348150G>A GRCh37
NC_000009.10:g.103387971G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6508C>T MANE Select ENSP00000355155.3:n.2767-6508C>T
ENST00000361820.3:c.2767-6508C>T ENSP00000355155.3:n.2767-6508C>T
NM_133445.2:c.2767-6508C>T NP_597702.2:n.2767-6508C>T
NM_133445.3:c.2767-6508C>T MANE Select NP_597702.2:n.2767-6508C>T