Canonical Allele Identifier: CA233009843

Gene: GRIN2B

Linked Data

• dbSNP Id: rs199731184
• MyVariant Identifiers: chr12:g.13761731T>C (hg19) ; chr12:g.13608797T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608797T>C , CM000674.2:g.13608797T>C	GRCh38
NC_000012.11:g.13761731T>C , CM000674.1:g.13761731T>C	GRCh37
NC_000012.10:g.13652998T>C	NCBI36
NG_031854.1:g.376292A>G
NG_031854.2:g.378216A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1816A>G MANE Select	ENSP00000477455.1:p.Ile606Val
ENST00000628166.2:n.76A>G
ENST00000609686.3:c.1816A>G	ENSP00000477455.1:p.Ile606Val
ENST00000628166.1:n.76A>G
NM_000834.3:c.1816A>G	NP_000825.2:p.Ile606Val
XM_011520628.1:c.1816A>G	XP_011518930.1:p.Ile606Val
XM_011520629.1:c.1816A>G	XP_011518931.1:p.Ile606Val
XM_011520630.1:c.1816A>G	XP_011518932.1:p.Ile606Val
XR_931372.1:n.179-6301T>C
XR_931373.1:n.318+40T>C
NM_000834.4:c.1816A>G	NP_000825.2:p.Ile606Val
XM_011520628.2:c.1816A>G	XP_011518930.1:p.Ile606Val
XM_011520629.2:c.1816A>G	XP_011518931.1:p.Ile606Val
XM_017019219.2:c.1816A>G	XP_016874708.1:p.Ile606Val
XR_001749013.1:n.457+40T>C
XR_931372.2:n.316-6301T>C
XR_931373.2:n.457+40T>C
NM_000834.5:c.1816A>G MANE Select	NP_000825.2:p.Ile606Val