Canonical Allele Identifier: CA478848594

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13717088G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564154G>C , CM000674.2:g.13564154G>C	GRCh38
NC_000012.11:g.13717088G>C , CM000674.1:g.13717088G>C	GRCh37
NC_000012.10:g.13608355G>C	NCBI36
NG_031854.1:g.420935C>G
NG_031854.2:g.422859C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3084C>G MANE Select	ENSP00000477455.1:p.Pro1028=
ENST00000637214.1:c.69+44449C>G	ENSP00000489997.1:n.69+44449C>G
ENST00000609686.3:c.3084C>G	ENSP00000477455.1:p.Pro1028=
ENST00000628166.1:n.1344C>G
NM_000834.3:c.3084C>G	NP_000825.2:p.Pro1028=
XM_005253351.2:c.870C>G	XP_005253408.1:p.Pro290=
XM_011520628.1:c.3084C>G	XP_011518930.1:p.Pro1028=
XM_011520629.1:c.3084C>G	XP_011518931.1:p.Pro1028=
XM_011520630.1:c.3084C>G	XP_011518932.1:p.Pro1028=
NM_000834.4:c.3084C>G	NP_000825.2:p.Pro1028=
XM_005253351.3:c.870C>G	XP_005253408.1:p.Pro290=
XM_011520628.2:c.3084C>G	XP_011518930.1:p.Pro1028=
XM_011520629.2:c.3084C>G	XP_011518931.1:p.Pro1028=
XM_017019219.2:c.3084C>G	XP_016874708.1:p.Pro1028=
NM_000834.5:c.3084C>G MANE Select	NP_000825.2:p.Pro1028=