Canonical Allele Identifier: CA1130086977
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs933984024

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139124G>T , CM000671.2:g.137139124G>T GRCh38
NC_000009.11:g.140033576G>T , CM000671.1:g.140033576G>T GRCh37
NC_000009.10:g.139153397G>T NCBI36
NG_011507.1:g.4968G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-363G>T ENSP00000360615.3:n.-363G>T
ENST00000371561.7:c.-363G>T ENSP00000360616.3:n.-363G>T
XM_005266073.3:c.-363G>T XP_005266130.1:n.-363G>T
XM_005266073.4:c.-363G>T XP_005266130.1:n.-363G>T