Canonical Allele Identifier: CA233009872

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 1291521
• ClinVar RCV Id: RCV001713458
• dbSNP Id: rs56069446
• gnomAD v2: 12-13761829-CA-C
• gnomAD v3: 12-13608895-CA-C
• gnomAD v4: 12-13608895-CA-C
• MyVariant Identifiers: chr12:g.13761830del (hg19) ; chr12:g.13608896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608898del , CM000674.2:g.13608898del	GRCh38
NC_000012.11:g.13761832del , CM000674.1:g.13761832del	GRCh37
NC_000012.10:g.13653099del	NCBI36
NG_031854.1:g.376193del
NG_031854.2:g.378117del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-64del MANE Select	ENSP00000477455.1:n.1781-64del
ENST00000628166.2:n.41-64del
ENST00000609686.3:c.1781-64del	ENSP00000477455.1:n.1781-64del
ENST00000628166.1:n.41-64del
NM_000834.3:c.1781-64del	NP_000825.2:n.1781-64del
XM_011520628.1:c.1781-64del	XP_011518930.1:n.1781-64del
XM_011520629.1:c.1781-64del	XP_011518931.1:n.1781-64del
XM_011520630.1:c.1781-64del	XP_011518932.1:n.1781-64del
XR_931372.1:n.179-6200del
XR_931373.1:n.318+141del
NM_000834.4:c.1781-64del	NP_000825.2:n.1781-64del
XM_011520628.2:c.1781-64del	XP_011518930.1:n.1781-64del
XM_011520629.2:c.1781-64del	XP_011518931.1:n.1781-64del
XM_017019219.2:c.1781-64del	XP_016874708.1:n.1781-64del
XR_001749013.1:n.457+141del
XR_931372.2:n.316-6200del
XR_931373.2:n.457+141del
NM_000834.5:c.1781-64del MANE Select	NP_000825.2:n.1781-64del