Canonical Allele Identifier: CA944999684

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1863142272
• gnomAD v3: 12-13981743-C-T
• gnomAD v4: 12-13981743-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981743C>T , CM000674.2:g.13981743C>T	GRCh38
NC_000012.11:g.14134677C>T , CM000674.1:g.14134677C>T	GRCh37
NC_000012.10:g.14025944C>T	NCBI36
NG_031854.1:g.3346G>A
NG_031854.2:g.5270G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-682-167G>A	ENSP00000486677.2:n.-682-167G>A
ENST00000627535.2:c.-448+173G>A	ENSP00000486411.1:n.-448+173G>A
ENST00000630791.1:c.-682-167G>A	ENSP00000486677.1:n.-682-167G>A
XM_011520629.1:c.-682-167G>A	XP_011518931.1:n.-682-167G>A
XM_011520628.2:c.-849G>A	XP_011518930.1:n.-849G>A
XM_011520629.2:c.-682-167G>A	XP_011518931.1:n.-682-167G>A