Canonical Allele Identifier: CA10603239
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 279975
dbSNP Id: rs886041295

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13615221T>C , CM000674.2:g.13615221T>C GRCh38
NC_000012.11:g.13768155T>C , CM000674.1:g.13768155T>C GRCh37
NC_000012.10:g.13659422T>C NCBI36
NG_031854.1:g.369868A>G
NG_031854.2:g.371792A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.1547A>G MANE Select ENSP00000477455.1:p.Asn516Ser
ENST00000609686.3:c.1547A>G ENSP00000477455.1:p.Asn516Ser
NM_000834.3:c.1547A>G NP_000825.2:p.Asn516Ser
XM_011520628.1:c.1547A>G XP_011518930.1:p.Asn516Ser
XM_011520629.1:c.1547A>G XP_011518931.1:p.Asn516Ser
XM_011520630.1:c.1547A>G XP_011518932.1:p.Asn516Ser
XR_931372.1:n.302T>C
XR_931373.1:n.442T>C
XR_931374.1:n.241T>C
NM_000834.4:c.1547A>G NP_000825.2:p.Asn516Ser
XM_011520628.2:c.1547A>G XP_011518930.1:p.Asn516Ser
XM_011520629.2:c.1547A>G XP_011518931.1:p.Asn516Ser
XM_017019219.2:c.1547A>G XP_016874708.1:p.Asn516Ser
XR_001749013.1:n.723T>C
XR_931372.2:n.439T>C
XR_931373.2:n.581T>C
NM_000834.5:c.1547A>G MANE Select NP_000825.2:p.Asn516Ser