Canonical Allele Identifier: CA1130086975
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1483013598

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139087G>C , CM000671.2:g.137139087G>C GRCh38
NC_000009.11:g.140033539G>C , CM000671.1:g.140033539G>C GRCh37
NC_000009.10:g.139153360G>C NCBI36
NG_011507.1:g.4931G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-400G>C ENSP00000360615.3:n.-400G>C
ENST00000371561.7:c.-400G>C ENSP00000360616.3:n.-400G>C