Canonical Allele Identifier: CA653982669

Gene: GRIN2B

Linked Data

• COSMIC: COSN22849593

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608970del , CM000674.2:g.13608970del	GRCh38
NC_000012.11:g.13761904del , CM000674.1:g.13761904del	GRCh37
NC_000012.10:g.13653171del	NCBI36
NG_031854.1:g.376122del
NG_031854.2:g.378046del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-135del MANE Select	ENSP00000477455.1:n.1781-135del
ENST00000628166.2:n.41-135del
ENST00000609686.3:c.1781-135del	ENSP00000477455.1:n.1781-135del
ENST00000628166.1:n.41-135del
NM_000834.3:c.1781-135del	NP_000825.2:n.1781-135del
XM_011520628.1:c.1781-135del	XP_011518930.1:n.1781-135del
XM_011520629.1:c.1781-135del	XP_011518931.1:n.1781-135del
XM_011520630.1:c.1781-135del	XP_011518932.1:n.1781-135del
XR_931372.1:n.179-6128del
XR_931373.1:n.318+213del
NM_000834.4:c.1781-135del	NP_000825.2:n.1781-135del
XM_011520628.2:c.1781-135del	XP_011518930.1:n.1781-135del
XM_011520629.2:c.1781-135del	XP_011518931.1:n.1781-135del
XM_017019219.2:c.1781-135del	XP_016874708.1:n.1781-135del
XR_001749013.1:n.457+213del
XR_931372.2:n.316-6128del
XR_931373.2:n.457+213del
NM_000834.5:c.1781-135del MANE Select	NP_000825.2:n.1781-135del