Canonical Allele Identifier: CA603467497

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1013298708
• gnomAD v2: 12-14134672-A-G
• gnomAD v3: 12-13981738-A-G
• gnomAD v4: 12-13981738-A-G
• MyVariant Identifiers: chr12:g.14134672A>G (hg19) ; chr12:g.13981738A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981738A>G , CM000674.2:g.13981738A>G	GRCh38
NC_000012.11:g.14134672A>G , CM000674.1:g.14134672A>G	GRCh37
NC_000012.10:g.14025939A>G	NCBI36
NG_031854.1:g.3351T>C
NG_031854.2:g.5275T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000630791.2:c.-682-162T>C	ENSP00000486677.2:n.-682-162T>C
ENST00000627535.2:c.-448+178T>C	ENSP00000486411.1:n.-448+178T>C
ENST00000630791.1:c.-682-162T>C	ENSP00000486677.1:n.-682-162T>C
XM_011520629.1:c.-682-162T>C	XP_011518931.1:n.-682-162T>C
XM_011520628.2:c.-844T>C	XP_011518930.1:n.-844T>C
XM_011520629.2:c.-682-162T>C	XP_011518931.1:n.-682-162T>C