Canonical Allele Identifier: CA2617750518

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13611624-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611626dup , CM000674.2:g.13611626dup	GRCh38
NC_000012.11:g.13764560dup , CM000674.1:g.13764560dup	GRCh37
NC_000012.10:g.13655827dup	NCBI36
NG_031854.1:g.373464dup
NG_031854.2:g.375388dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1780+100dup MANE Select	ENSP00000477455.1:n.1780+100dup
ENST00000609686.3:c.1780+100dup	ENSP00000477455.1:n.1780+100dup
NM_000834.3:c.1780+100dup	NP_000825.2:n.1780+100dup
XM_011520628.1:c.1780+100dup	XP_011518930.1:n.1780+100dup
XM_011520629.1:c.1780+100dup	XP_011518931.1:n.1780+100dup
XM_011520630.1:c.1780+100dup	XP_011518932.1:n.1780+100dup
XR_931372.1:n.179-3472dup
XR_931373.1:n.318+2869dup
XR_931374.1:n.117+1026dup
NM_000834.4:c.1780+100dup	NP_000825.2:n.1780+100dup
XM_011520628.2:c.1780+100dup	XP_011518930.1:n.1780+100dup
XM_011520629.2:c.1780+100dup	XP_011518931.1:n.1780+100dup
XM_017019219.2:c.1780+100dup	XP_016874708.1:n.1780+100dup
XR_001749013.1:n.599+1026dup
XR_931372.2:n.316-3472dup
XR_931373.2:n.457+2869dup
NM_000834.5:c.1780+100dup MANE Select	NP_000825.2:n.1780+100dup