Canonical Allele Identifier: CA2725500815

Gene: GRIN2B

Linked Data

• dbSNP Id: rs2136470117

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608562G>C , CM000674.2:g.13608562G>C	GRCh38
NC_000012.11:g.13761496G>C , CM000674.1:g.13761496G>C	GRCh37
NC_000012.10:g.13652763G>C	NCBI36
NG_031854.1:g.376527C>G
NG_031854.2:g.378451C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2010+41C>G MANE Select	ENSP00000477455.1:n.2010+41C>G
ENST00000628166.2:n.270+41C>G
ENST00000637214.1:c.69+41C>G	ENSP00000489997.1:n.69+41C>G
ENST00000609686.3:c.2010+41C>G	ENSP00000477455.1:n.2010+41C>G
ENST00000628166.1:n.270+41C>G
NM_000834.3:c.2010+41C>G	NP_000825.2:n.2010+41C>G
XM_005253351.2:c.-44+41C>G	XP_005253408.1:n.-44+41C>G
XM_011520628.1:c.2010+41C>G	XP_011518930.1:n.2010+41C>G
XM_011520629.1:c.2010+41C>G	XP_011518931.1:n.2010+41C>G
XM_011520630.1:c.2010+41C>G	XP_011518932.1:n.2010+41C>G
XR_931372.1:n.179-6536G>C
XR_931373.1:n.179-56G>C
NM_000834.4:c.2010+41C>G	NP_000825.2:n.2010+41C>G
XM_005253351.3:c.-44+41C>G	XP_005253408.1:n.-44+41C>G
XM_011520628.2:c.2010+41C>G	XP_011518930.1:n.2010+41C>G
XM_011520629.2:c.2010+41C>G	XP_011518931.1:n.2010+41C>G
XM_017019219.2:c.2010+41C>G	XP_016874708.1:n.2010+41C>G
XR_001749013.1:n.318-56G>C
XR_931372.2:n.316-6536G>C
XR_931373.2:n.318-56G>C
NM_000834.5:c.2010+41C>G MANE Select	NP_000825.2:n.2010+41C>G