Canonical Allele Identifier: CA685661385

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1322382032
• gnomAD v3: 12-13562284-G-C
• gnomAD v4: 12-13562284-G-C
• MyVariant Identifiers: chr12:g.13715218G>C (hg19) ; chr12:g.13562284G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562284G>C , CM000674.2:g.13562284G>C	GRCh38
NC_000012.11:g.13715218G>C , CM000674.1:g.13715218G>C	GRCh37
NC_000012.10:g.13606485G>C	NCBI36
NG_031854.1:g.422805C>G
NG_031854.2:g.424729C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*499C>G MANE Select	ENSP00000477455.1:n.*499C>G
ENST00000636207.1:n.8C>G
ENST00000637214.1:c.69+46319C>G	ENSP00000489997.1:n.69+46319C>G
ENST00000609686.3:c.*499C>G	ENSP00000477455.1:n.*499C>G
NM_000834.3:c.*499C>G	NP_000825.2:n.*499C>G
XM_005253351.2:c.*499C>G	XP_005253408.1:n.*499C>G
XM_011520628.1:c.*499C>G	XP_011518930.1:n.*499C>G
XM_011520629.1:c.*499C>G	XP_011518931.1:n.*499C>G
XM_011520630.1:c.*499C>G	XP_011518932.1:n.*499C>G
NM_000834.4:c.*499C>G	NP_000825.2:n.*499C>G
XM_005253351.3:c.*499C>G	XP_005253408.1:n.*499C>G
XM_011520628.2:c.*499C>G	XP_011518930.1:n.*499C>G
XM_011520629.2:c.*499C>G	XP_011518931.1:n.*499C>G
XM_017019219.2:c.*499C>G	XP_016874708.1:n.*499C>G
NM_000834.5:c.*499C>G MANE Select	NP_000825.2:n.*499C>G