Canonical Allele Identifier: CA591214842
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs1483013598
gnomAD v2: 9-140033539-G-T
MyVariant Identifiers: chr9:g.140033539G>T (hg19) chr9:g.137139087G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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