Canonical Allele Identifier: CA201726951
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs931089924

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137138536A>C , CM000671.2:g.137138536A>C GRCh38
NC_000009.11:g.140032988A>C , CM000671.1:g.140032988A>C GRCh37
NC_000009.10:g.139152809A>C NCBI36
NG_011507.1:g.4380A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371560.5:c.-951A>C ENSP00000360615.3:n.-951A>C
ENST00000371561.7:c.-951A>C ENSP00000360616.3:n.-951A>C