Canonical Allele Identifier: CA6460940
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs751021224

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13564100G>A , CM000674.2:g.13564100G>A GRCh38
NC_000012.11:g.13717034G>A , CM000674.1:g.13717034G>A GRCh37
NC_000012.10:g.13608301G>A NCBI36
NG_031854.1:g.420989C>T
NG_031854.2:g.422913C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.3138C>T MANE Select ENSP00000477455.1:p.Ser1046=
ENST00000637214.1:c.69+44503C>T ENSP00000489997.1:n.69+44503C>T
ENST00000609686.3:c.3138C>T ENSP00000477455.1:p.Ser1046=
ENST00000628166.1:n.1398C>T
NM_000834.3:c.3138C>T NP_000825.2:p.Ser1046=
XM_005253351.2:c.924C>T XP_005253408.1:p.Ser308=
XM_011520628.1:c.3138C>T XP_011518930.1:p.Ser1046=
XM_011520629.1:c.3138C>T XP_011518931.1:p.Ser1046=
XM_011520630.1:c.3138C>T XP_011518932.1:p.Ser1046=
NM_000834.4:c.3138C>T NP_000825.2:p.Ser1046=
XM_005253351.3:c.924C>T XP_005253408.1:p.Ser308=
XM_011520628.2:c.3138C>T XP_011518930.1:p.Ser1046=
XM_011520629.2:c.3138C>T XP_011518931.1:p.Ser1046=
XM_017019219.2:c.3138C>T XP_016874708.1:p.Ser1046=
NM_000834.5:c.3138C>T MANE Select NP_000825.2:p.Ser1046=