Canonical Allele Identifier: CA1868339580
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585898A= , CM000671.2:g.101585898A= GRCh38
NC_000009.11:g.104348180A= , CM000671.1:g.104348180A= GRCh37
NC_000009.10:g.103388001A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6538T= MANE Select ENSP00000355155.3:n.2767-6538T=
ENST00000361820.3:c.2767-6538T= ENSP00000355155.3:n.2767-6538T=
NM_133445.2:c.2767-6538T= NP_597702.2:n.2767-6538T=
NM_133445.3:c.2767-6538T= MANE Select NP_597702.2:n.2767-6538T=