Canonical Allele Identifier: CA478848512

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13716992G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564058G>C , CM000674.2:g.13564058G>C	GRCh38
NC_000012.11:g.13716992G>C , CM000674.1:g.13716992G>C	GRCh37
NC_000012.10:g.13608259G>C	NCBI36
NG_031854.1:g.421031C>G
NG_031854.2:g.422955C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3180C>G MANE Select	ENSP00000477455.1:p.Val1060=
ENST00000637214.1:c.69+44545C>G	ENSP00000489997.1:n.69+44545C>G
ENST00000609686.3:c.3180C>G	ENSP00000477455.1:p.Val1060=
ENST00000628166.1:n.1440C>G
NM_000834.3:c.3180C>G	NP_000825.2:p.Val1060=
XM_005253351.2:c.966C>G	XP_005253408.1:p.Val322=
XM_011520628.1:c.3180C>G	XP_011518930.1:p.Val1060=
XM_011520629.1:c.3180C>G	XP_011518931.1:p.Val1060=
XM_011520630.1:c.3180C>G	XP_011518932.1:p.Val1060=
NM_000834.4:c.3180C>G	NP_000825.2:p.Val1060=
XM_005253351.3:c.966C>G	XP_005253408.1:p.Val322=
XM_011520628.2:c.3180C>G	XP_011518930.1:p.Val1060=
XM_011520629.2:c.3180C>G	XP_011518931.1:p.Val1060=
XM_017019219.2:c.3180C>G	XP_016874708.1:p.Val1060=
NM_000834.5:c.3180C>G MANE Select	NP_000825.2:p.Val1060=