Canonical Allele Identifier: CA1884318150
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1832029942

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139142T>C , CM000671.2:g.137139142T>C GRCh38
NC_000009.11:g.140033594T>C , CM000671.1:g.140033594T>C GRCh37
NC_000009.10:g.139153415T>C NCBI36
NG_011507.1:g.4986T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-345T>C ENSP00000360615.3:n.-345T>C
ENST00000371561.7:c.-345T>C ENSP00000360616.3:n.-345T>C
XM_005266073.3:c.-345T>C XP_005266130.1:n.-345T>C
XM_005266073.4:c.-345T>C XP_005266130.1:n.-345T>C