Canonical Allele Identifier: CA478771546

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13764732G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611798G>T , CM000674.2:g.13611798G>T	GRCh38
NC_000012.11:g.13764732G>T , CM000674.1:g.13764732G>T	GRCh37
NC_000012.10:g.13655999G>T	NCBI36
NG_031854.1:g.373291C>A
NG_031854.2:g.375215C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1707C>A MANE Select	ENSP00000477455.1:p.Val569=
ENST00000609686.3:c.1707C>A	ENSP00000477455.1:p.Val569=
NM_000834.3:c.1707C>A	NP_000825.2:p.Val569=
XM_011520628.1:c.1707C>A	XP_011518930.1:p.Val569=
XM_011520629.1:c.1707C>A	XP_011518931.1:p.Val569=
XM_011520630.1:c.1707C>A	XP_011518932.1:p.Val569=
XR_931372.1:n.179-3300G>T
XR_931373.1:n.318+3041G>T
XR_931374.1:n.117+1198G>T
NM_000834.4:c.1707C>A	NP_000825.2:p.Val569=
XM_011520628.2:c.1707C>A	XP_011518930.1:p.Val569=
XM_011520629.2:c.1707C>A	XP_011518931.1:p.Val569=
XM_017019219.2:c.1707C>A	XP_016874708.1:p.Val569=
XR_001749013.1:n.599+1198G>T
XR_931372.2:n.316-3300G>T
XR_931373.2:n.457+3041G>T
NM_000834.5:c.1707C>A MANE Select	NP_000825.2:p.Val569=