Canonical Allele Identifier: CA2617718473

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13562575-GGAGAGAACTGTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562576_13562588del , CM000674.2:g.13562576_13562588del	GRCh38
NC_000012.11:g.13715510_13715522del , CM000674.1:g.13715510_13715522del	GRCh37
NC_000012.10:g.13606777_13606789del	NCBI36
NG_031854.1:g.422501_422513del
NG_031854.2:g.424425_424437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*195_*207del MANE Select	ENSP00000477455.1:n.*195_*207del
ENST00000637214.1:c.69+46015_69+46027del	ENSP00000489997.1:n.69+46015_69+46027del
ENST00000609686.3:c.*195_*207del	ENSP00000477455.1:n.*195_*207del
NM_000834.3:c.*195_*207del	NP_000825.2:n.*195_*207del
XM_005253351.2:c.*195_*207del	XP_005253408.1:n.*195_*207del
XM_011520628.1:c.*195_*207del	XP_011518930.1:n.*195_*207del
XM_011520629.1:c.*195_*207del	XP_011518931.1:n.*195_*207del
XM_011520630.1:c.*195_*207del	XP_011518932.1:n.*195_*207del
NM_000834.4:c.*195_*207del	NP_000825.2:n.*195_*207del
XM_005253351.3:c.*195_*207del	XP_005253408.1:n.*195_*207del
XM_011520628.2:c.*195_*207del	XP_011518930.1:n.*195_*207del
XM_011520629.2:c.*195_*207del	XP_011518931.1:n.*195_*207del
XM_017019219.2:c.*195_*207del	XP_016874708.1:n.*195_*207del
NM_000834.5:c.*195_*207del MANE Select	NP_000825.2:n.*195_*207del