Canonical Allele Identifier: CA1884318129
Gene: GRIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139099G= , CM000671.2:g.137139099G= GRCh38
NC_000009.11:g.140033551G= , CM000671.1:g.140033551G= GRCh37
NC_000009.10:g.139153372G= NCBI36
NG_011507.1:g.4943G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-388G= ENSP00000360615.3:n.-388G=
ENST00000371561.7:c.-388G= ENSP00000360616.3:n.-388G=
XM_005266073.4:c.-388G= XP_005266130.1:n.-388G=