Canonical Allele Identifier: CA174968
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 162085
ClinVar RCV Id: RCV000149503 RCV001172367
dbSNP Id: rs672601376
MyVariant Identifiers: chr12:g.13761694A>C (hg19) chr12:g.13608760A>C (hg38)
PubMed: PMID:24272827
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13608760A>C , CM000674.2:g.13608760A>C GRCh38
NC_000012.11:g.13761694A>C , CM000674.1:g.13761694A>C GRCh37
NC_000012.10:g.13652961A>C NCBI36
NG_031854.1:g.376329T>G
NG_031854.2:g.378253T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1853T>G MANE Select ENSP00000477455.1:p.Val618Gly
ENST00000628166.2:n.113T>G
ENST00000609686.3:c.1853T>G ENSP00000477455.1:p.Val618Gly
ENST00000628166.1:n.113T>G
NM_000834.3:c.1853T>G NP_000825.2:p.Val618Gly
XM_011520628.1:c.1853T>G XP_011518930.1:p.Val618Gly
XM_011520629.1:c.1853T>G XP_011518931.1:p.Val618Gly
XM_011520630.1:c.1853T>G XP_011518932.1:p.Val618Gly
XR_931372.1:n.179-6338A>C
XR_931373.1:n.318+3A>C
NM_000834.4:c.1853T>G NP_000825.2:p.Val618Gly
XM_011520628.2:c.1853T>G XP_011518930.1:p.Val618Gly
XM_011520629.2:c.1853T>G XP_011518931.1:p.Val618Gly
XM_017019219.2:c.1853T>G XP_016874708.1:p.Val618Gly
XR_001749013.1:n.457+3A>C
XR_931372.2:n.316-6338A>C
XR_931373.2:n.457+3A>C
NM_000834.5:c.1853T>G MANE Select NP_000825.2:p.Val618Gly
Search 100 bp 5'
Search 100 bp 3'