Canonical Allele Identifier: CA2617758463

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13981829-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981829G>T , CM000674.2:g.13981829G>T	GRCh38
NC_000012.11:g.14134763G>T , CM000674.1:g.14134763G>T	GRCh37
NC_000012.10:g.14026030G>T	NCBI36
NG_031854.1:g.3260C>A
NG_031854.2:g.5184C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-683+87C>A	ENSP00000486677.2:n.-683+87C>A
ENST00000627535.2:c.-448+87C>A	ENSP00000486411.1:n.-448+87C>A
ENST00000630791.1:c.-683+87C>A	ENSP00000486677.1:n.-683+87C>A
XM_011520629.1:c.-683+87C>A	XP_011518931.1:n.-683+87C>A
XM_011520628.2:c.-935C>A	XP_011518930.1:n.-935C>A
XM_011520629.2:c.-683+87C>A	XP_011518931.1:n.-683+87C>A