Canonical Allele Identifier: CA2617750500

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13611613-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611617del , CM000674.2:g.13611617del	GRCh38
NC_000012.11:g.13764551del , CM000674.1:g.13764551del	GRCh37
NC_000012.10:g.13655818del	NCBI36
NG_031854.1:g.373475del
NG_031854.2:g.375399del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1780+111del MANE Select	ENSP00000477455.1:n.1780+111del
ENST00000609686.3:c.1780+111del	ENSP00000477455.1:n.1780+111del
NM_000834.3:c.1780+111del	NP_000825.2:n.1780+111del
XM_011520628.1:c.1780+111del	XP_011518930.1:n.1780+111del
XM_011520629.1:c.1780+111del	XP_011518931.1:n.1780+111del
XM_011520630.1:c.1780+111del	XP_011518932.1:n.1780+111del
XR_931372.1:n.179-3481del
XR_931373.1:n.318+2860del
XR_931374.1:n.117+1017del
NM_000834.4:c.1780+111del	NP_000825.2:n.1780+111del
XM_011520628.2:c.1780+111del	XP_011518930.1:n.1780+111del
XM_011520629.2:c.1780+111del	XP_011518931.1:n.1780+111del
XM_017019219.2:c.1780+111del	XP_016874708.1:n.1780+111del
XR_001749013.1:n.599+1017del
XR_931372.2:n.316-3481del
XR_931373.2:n.457+2860del
NM_000834.5:c.1780+111del MANE Select	NP_000825.2:n.1780+111del