Canonical Allele Identifier: CA478853972

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.14019089G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866155G>C , CM000674.2:g.13866155G>C	GRCh38
NC_000012.11:g.14019089G>C , CM000674.1:g.14019089G>C	GRCh37
NC_000012.10:g.13910356G>C	NCBI36
NG_031854.1:g.118934C>G
NG_031854.2:g.120858C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.54C>G MANE Select	ENSP00000477455.1:p.Val18=
ENST00000630791.2:c.54C>G	ENSP00000486677.2:p.Val18=
ENST00000609686.3:c.54C>G	ENSP00000477455.1:p.Val18=
ENST00000627535.2:c.54C>G	ENSP00000486411.1:p.Val18=
ENST00000630791.1:c.54C>G	ENSP00000486677.1:p.Val18=
NM_000834.3:c.54C>G	NP_000825.2:p.Val18=
XM_011520628.1:c.54C>G	XP_011518930.1:p.Val18=
XM_011520629.1:c.54C>G	XP_011518931.1:p.Val18=
XM_011520630.1:c.54C>G	XP_011518932.1:p.Val18=
NM_000834.4:c.54C>G	NP_000825.2:p.Val18=
XM_011520628.2:c.54C>G	XP_011518930.1:p.Val18=
XM_011520629.2:c.54C>G	XP_011518931.1:p.Val18=
XM_017019219.2:c.54C>G	XP_016874708.1:p.Val18=
NM_000834.5:c.54C>G MANE Select	NP_000825.2:p.Val18=