Canonical Allele Identifier: CA685703337

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1431423747
• gnomAD v4: 12-13981719-G-A
• MyVariant Identifiers: chr12:g.14134653G>A (hg19) ; chr12:g.13981719G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981719G>A , CM000674.2:g.13981719G>A	GRCh38
NC_000012.11:g.14134653G>A , CM000674.1:g.14134653G>A	GRCh37
NC_000012.10:g.14025920G>A	NCBI36
NG_031854.1:g.3370C>T
NG_031854.2:g.5294C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000630791.2:c.-682-143C>T	ENSP00000486677.2:n.-682-143C>T
ENST00000627535.2:c.-448+197C>T	ENSP00000486411.1:n.-448+197C>T
ENST00000630791.1:c.-682-143C>T	ENSP00000486677.1:n.-682-143C>T
XM_011520629.1:c.-682-143C>T	XP_011518931.1:n.-682-143C>T
XM_011520628.2:c.-825C>T	XP_011518930.1:n.-825C>T
XM_011520629.2:c.-682-143C>T	XP_011518931.1:n.-682-143C>T