Canonical Allele Identifier: CA6461486

Gene: GRIN2B

Linked Data

• dbSNP Id: rs754803710
• ExAC: 12:14019170 CA / C
• gnomAD v2: 12-14019170-CA-C
• gnomAD v4: 12-13866236-CA-C
• MyVariant Identifiers: chr12:g.14019171del (hg19) ; chr12:g.13866237del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866239del , CM000674.2:g.13866239del	GRCh38
NC_000012.11:g.14019173del , CM000674.1:g.14019173del	GRCh37
NC_000012.10:g.13910440del	NCBI36
NG_031854.1:g.118852del
NG_031854.2:g.120776del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-18-11del MANE Select	ENSP00000477455.1:n.-18-11del
ENST00000630791.2:c.-18-11del	ENSP00000486677.2:n.-18-11del
ENST00000609686.3:c.-18-11del	ENSP00000477455.1:n.-18-11del
ENST00000627535.2:c.-18-11del	ENSP00000486411.1:n.-18-11del
ENST00000630791.1:c.-18-11del	ENSP00000486677.1:n.-18-11del
NM_000834.3:c.-18-11del	NP_000825.2:n.-18-11del
XM_011520628.1:c.-18-11del	XP_011518930.1:n.-18-11del
XM_011520629.1:c.-18-11del	XP_011518931.1:n.-18-11del
XM_011520630.1:c.-18-11del	XP_011518932.1:n.-18-11del
NM_000834.4:c.-18-11del	NP_000825.2:n.-18-11del
XM_011520628.2:c.-18-11del	XP_011518930.1:n.-18-11del
XM_011520629.2:c.-18-11del	XP_011518931.1:n.-18-11del
XM_017019219.2:c.-18-11del	XP_016874708.1:n.-18-11del
NM_000834.5:c.-18-11del MANE Select	NP_000825.2:n.-18-11del