Canonical Allele Identifier: CA478853867
Gene: GRIN2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.14018930T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13865996T>G , CM000674.2:g.13865996T>G GRCh38
NC_000012.11:g.14018930T>G , CM000674.1:g.14018930T>G GRCh37
NC_000012.10:g.13910197T>G NCBI36
NG_031854.1:g.119093A>C
NG_031854.2:g.121017A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.213A>C MANE Select ENSP00000477455.1:p.Val71=
ENST00000630791.2:c.213A>C ENSP00000486677.2:p.Val71=
ENST00000609686.3:c.213A>C ENSP00000477455.1:p.Val71=
NM_000834.3:c.213A>C NP_000825.2:p.Val71=
XM_011520628.1:c.213A>C XP_011518930.1:p.Val71=
XM_011520629.1:c.213A>C XP_011518931.1:p.Val71=
XM_011520630.1:c.213A>C XP_011518932.1:p.Val71=
NM_000834.4:c.213A>C NP_000825.2:p.Val71=
XM_011520628.2:c.213A>C XP_011518930.1:p.Val71=
XM_011520629.2:c.213A>C XP_011518931.1:p.Val71=
XM_017019219.2:c.213A>C XP_016874708.1:p.Val71=
NM_000834.5:c.213A>C MANE Select NP_000825.2:p.Val71=