Canonical Allele Identifier: CA2617758461

Gene: GRIN2B

Linked Data

• dbSNP Id: rs2136884163
• gnomAD v4: 12-13981827-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981827C>T , CM000674.2:g.13981827C>T	GRCh38
NC_000012.11:g.14134761C>T , CM000674.1:g.14134761C>T	GRCh37
NC_000012.10:g.14026028C>T	NCBI36
NG_031854.1:g.3262G>A
NG_031854.2:g.5186G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-683+89G>A	ENSP00000486677.2:n.-683+89G>A
ENST00000627535.2:c.-448+89G>A	ENSP00000486411.1:n.-448+89G>A
ENST00000630791.1:c.-683+89G>A	ENSP00000486677.1:n.-683+89G>A
XM_011520629.1:c.-683+89G>A	XP_011518931.1:n.-683+89G>A
XM_011520628.2:c.-933G>A	XP_011518930.1:n.-933G>A
XM_011520629.2:c.-683+89G>A	XP_011518931.1:n.-683+89G>A