Canonical Allele Identifier: CA174969
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 162086
ClinVar RCV Id: RCV000149504 RCV001172364
dbSNP Id: rs672601377
MyVariant Identifiers: chr12:g.13761703T>A (hg19) chr12:g.13608769T>A (hg38)
PubMed: PMID:24272827
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13608769T>A , CM000674.2:g.13608769T>A GRCh38
NC_000012.11:g.13761703T>A , CM000674.1:g.13761703T>A GRCh37
NC_000012.10:g.13652970T>A NCBI36
NG_031854.1:g.376320A>T
NG_031854.2:g.378244A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1844A>T MANE Select ENSP00000477455.1:p.Asn615Ile
ENST00000628166.2:n.104A>T
ENST00000609686.3:c.1844A>T ENSP00000477455.1:p.Asn615Ile
ENST00000628166.1:n.104A>T
NM_000834.3:c.1844A>T NP_000825.2:p.Asn615Ile
XM_011520628.1:c.1844A>T XP_011518930.1:p.Asn615Ile
XM_011520629.1:c.1844A>T XP_011518931.1:p.Asn615Ile
XM_011520630.1:c.1844A>T XP_011518932.1:p.Asn615Ile
XR_931372.1:n.179-6329T>A
XR_931373.1:n.318+12T>A
NM_000834.4:c.1844A>T NP_000825.2:p.Asn615Ile
XM_011520628.2:c.1844A>T XP_011518930.1:p.Asn615Ile
XM_011520629.2:c.1844A>T XP_011518931.1:p.Asn615Ile
XM_017019219.2:c.1844A>T XP_016874708.1:p.Asn615Ile
XR_001749013.1:n.457+12T>A
XR_931372.2:n.316-6329T>A
XR_931373.2:n.457+12T>A
NM_000834.5:c.1844A>T MANE Select NP_000825.2:p.Asn615Ile
Search 100 bp 5'
Search 100 bp 3'