Canonical Allele Identifier: CA16043466
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 373959
ClinVar RCV Id: RCV000414776
dbSNP Id: rs1057518800

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13567228C>T , CM000674.2:g.13567228C>T GRCh38
NC_000012.11:g.13720162C>T , CM000674.1:g.13720162C>T GRCh37
NC_000012.10:g.13611429C>T NCBI36
NG_031854.1:g.417861G>A
NG_031854.2:g.419785G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.2395G>A MANE Select ENSP00000477455.1:p.Gly799Ser
ENST00000628166.2:n.655G>A
ENST00000637214.1:c.69+41375G>A ENSP00000489997.1:n.69+41375G>A
ENST00000609686.3:c.2395G>A ENSP00000477455.1:p.Gly799Ser
ENST00000628166.1:n.655G>A
NM_000834.3:c.2395G>A NP_000825.2:p.Gly799Ser
XM_005253351.2:c.181G>A XP_005253408.1:p.Gly61Ser
XM_011520628.1:c.2395G>A XP_011518930.1:p.Gly799Ser
XM_011520629.1:c.2395G>A XP_011518931.1:p.Gly799Ser
XM_011520630.1:c.2395G>A XP_011518932.1:p.Gly799Ser
NM_000834.4:c.2395G>A NP_000825.2:p.Gly799Ser
XM_005253351.3:c.181G>A XP_005253408.1:p.Gly61Ser
XM_011520628.2:c.2395G>A XP_011518930.1:p.Gly799Ser
XM_011520629.2:c.2395G>A XP_011518931.1:p.Gly799Ser
XM_017019219.2:c.2395G>A XP_016874708.1:p.Gly799Ser
NM_000834.5:c.2395G>A MANE Select NP_000825.2:p.Gly799Ser