Canonical Allele Identifier: CA1868339675
Gene: GRIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101586130C= , CM000671.2:g.101586130C= GRCh38
NC_000009.11:g.104348412C= , CM000671.1:g.104348412C= GRCh37
NC_000009.10:g.103388233C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6770G= MANE Select ENSP00000355155.3:n.2767-6770G=
ENST00000361820.3:c.2767-6770G= ENSP00000355155.3:n.2767-6770G=
NM_133445.2:c.2767-6770G= NP_597702.2:n.2767-6770G=
NM_133445.3:c.2767-6770G= MANE Select NP_597702.2:n.2767-6770G=