Canonical Allele Identifier: CA2617758378

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13981709-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981711del , CM000674.2:g.13981711del	GRCh38
NC_000012.11:g.14134645del , CM000674.1:g.14134645del	GRCh37
NC_000012.10:g.14025912del	NCBI36
NG_031854.1:g.3379del
NG_031854.2:g.5303del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-682-134del	ENSP00000486677.2:n.-682-134del
ENST00000627535.2:c.-448+206del	ENSP00000486411.1:n.-448+206del
ENST00000630791.1:c.-682-134del	ENSP00000486677.1:n.-682-134del
XM_011520629.1:c.-682-134del	XP_011518931.1:n.-682-134del
XM_011520628.2:c.-816del	XP_011518930.1:n.-816del
XM_011520629.2:c.-682-134del	XP_011518931.1:n.-682-134del