Canonical Allele Identifier: CA1868339537
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1827944298

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585810G>A , CM000671.2:g.101585810G>A GRCh38
NC_000009.11:g.104348092G>A , CM000671.1:g.104348092G>A GRCh37
NC_000009.10:g.103387913G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6450C>T MANE Select ENSP00000355155.3:n.2767-6450C>T
ENST00000361820.3:c.2767-6450C>T ENSP00000355155.3:n.2767-6450C>T
NM_133445.2:c.2767-6450C>T NP_597702.2:n.2767-6450C>T
NM_133445.3:c.2767-6450C>T MANE Select NP_597702.2:n.2767-6450C>T