Canonical Allele Identifier: CA197290860
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs139579340

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585917A>G , CM000671.2:g.101585917A>G GRCh38
NC_000009.11:g.104348199A>G , CM000671.1:g.104348199A>G GRCh37
NC_000009.10:g.103388020A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6557T>C MANE Select ENSP00000355155.3:n.2767-6557T>C
ENST00000361820.3:c.2767-6557T>C ENSP00000355155.3:n.2767-6557T>C
NM_133445.2:c.2767-6557T>C NP_597702.2:n.2767-6557T>C
NM_133445.3:c.2767-6557T>C MANE Select NP_597702.2:n.2767-6557T>C