Canonical Allele Identifier: CA201727227
Gene: GRIN1 HGNC NCBI

Linked Data

dbSNP Id: rs922312938
gnomAD v2: 9-140033598-C-T
gnomAD v3: 9-137139146-C-T
gnomAD v4: 9-137139146-C-T
MyVariant Identifiers: chr9:g.140033598C>T (hg19) chr9:g.137139146C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137139146C>T , CM000671.2:g.137139146C>T GRCh38
NC_000009.11:g.140033598C>T , CM000671.1:g.140033598C>T GRCh37
NC_000009.10:g.139153419C>T NCBI36
NG_011507.1:g.4990C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371560.5:c.-341C>T ENSP00000360615.3:n.-341C>T
ENST00000371561.7:c.-341C>T ENSP00000360616.3:n.-341C>T
XM_005266073.3:c.-341C>T XP_005266130.1:n.-341C>T
XM_005266073.4:c.-341C>T XP_005266130.1:n.-341C>T
Search 100 bp 5'
Search 100 bp 3'