Canonical Allele Identifier: CA130437
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 39659
ClinVar RCV Id: RCV000032863
dbSNP Id: rs398122824

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13570019T>C , CM000674.2:g.13570019T>C GRCh38
NC_000012.11:g.13722953T>C , CM000674.1:g.13722953T>C GRCh37
NC_000012.10:g.13614220T>C NCBI36
NG_031854.1:g.415070A>G
NG_031854.2:g.416994A>G

Transcript Alleles

HGVS Amino-acid change
NM_000834.3:c.2172-2A>G VV NP_000825.2:p.=
XM_005253351.2:c.-43-2A>G XP_005253408.1:p.=
XM_011520628.1:c.2172-2A>G XP_011518930.1:p.=
XM_011520629.1:c.2172-2A>G XP_011518931.1:p.=
XM_011520630.1:c.2172-2A>G XP_011518932.1:p.=
NM_000834.4:c.2172-2A>G VV
XM_005253351.3:c.-43-2A>G
XM_011520628.2:c.2172-2A>G
XM_011520629.2:c.2172-2A>G
XM_017019219.2:c.2172-2A>G XP_016874708.1:p.=
ENST00000609686.3:c.2172-2A>G ENSP00000477455.1:p.=
ENST00000628166.1:n.432-2A>G