Canonical Allele Identifier: CA2617757469

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13754055-CAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13754058_13754060del , CM000674.2:g.13754058_13754060del	GRCh38
NC_000012.11:g.13906992_13906994del , CM000674.1:g.13906992_13906994del	GRCh37
NC_000012.10:g.13798259_13798261del	NCBI36
NG_031854.1:g.231031_231033del
NG_031854.2:g.232955_232957del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-143_412-141del MANE Select	ENSP00000477455.1:n.412-143_412-141del
ENST00000630791.2:c.412-143_412-141del	ENSP00000486677.2:n.412-143_412-141del
ENST00000609686.3:c.412-143_412-141del	ENSP00000477455.1:n.412-143_412-141del
NM_000834.3:c.412-143_412-141del	NP_000825.2:n.412-143_412-141del
XM_011520628.1:c.412-143_412-141del	XP_011518930.1:n.412-143_412-141del
XM_011520629.1:c.412-143_412-141del	XP_011518931.1:n.412-143_412-141del
XM_011520630.1:c.412-143_412-141del	XP_011518932.1:n.412-143_412-141del
NM_000834.4:c.412-143_412-141del	NP_000825.2:n.412-143_412-141del
XM_011520628.2:c.412-143_412-141del	XP_011518930.1:n.412-143_412-141del
XM_011520629.2:c.412-143_412-141del	XP_011518931.1:n.412-143_412-141del
XM_017019219.2:c.412-143_412-141del	XP_016874708.1:n.412-143_412-141del
NM_000834.5:c.412-143_412-141del MANE Select	NP_000825.2:n.412-143_412-141del