Canonical Allele Identifier: CA653204788
Gene: GRIN3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585895G>T , CM000671.2:g.101585895G>T GRCh38
NC_000009.11:g.104348177G>T , CM000671.1:g.104348177G>T GRCh37
NC_000009.10:g.103387998G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6535C>A MANE Select ENSP00000355155.3:n.2767-6535C>A
ENST00000361820.3:c.2767-6535C>A ENSP00000355155.3:n.2767-6535C>A
NM_133445.2:c.2767-6535C>A NP_597702.2:n.2767-6535C>A
NM_133445.3:c.2767-6535C>A MANE Select NP_597702.2:n.2767-6535C>A