Canonical Allele Identifier: CA1868339548
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs893692471

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585837C>A , CM000671.2:g.101585837C>A GRCh38
NC_000009.11:g.104348119C>A , CM000671.1:g.104348119C>A GRCh37
NC_000009.10:g.103387940C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6477G>T MANE Select ENSP00000355155.3:n.2767-6477G>T
ENST00000361820.3:c.2767-6477G>T ENSP00000355155.3:n.2767-6477G>T
NM_133445.2:c.2767-6477G>T NP_597702.2:n.2767-6477G>T
NM_133445.3:c.2767-6477G>T MANE Select NP_597702.2:n.2767-6477G>T