Canonical Allele Identifier: CA233010376

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1045230787
• gnomAD v3: 12-13611658-G-A
• gnomAD v4: 12-13611658-G-A
• MyVariant Identifiers: chr12:g.13764592G>A (hg19) ; chr12:g.13611658G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611658G>A , CM000674.2:g.13611658G>A	GRCh38
NC_000012.11:g.13764592G>A , CM000674.1:g.13764592G>A	GRCh37
NC_000012.10:g.13655859G>A	NCBI36
NG_031854.1:g.373431C>T
NG_031854.2:g.375355C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1780+67C>T MANE Select	ENSP00000477455.1:n.1780+67C>T
ENST00000609686.3:c.1780+67C>T	ENSP00000477455.1:n.1780+67C>T
NM_000834.3:c.1780+67C>T	NP_000825.2:n.1780+67C>T
XM_011520628.1:c.1780+67C>T	XP_011518930.1:n.1780+67C>T
XM_011520629.1:c.1780+67C>T	XP_011518931.1:n.1780+67C>T
XM_011520630.1:c.1780+67C>T	XP_011518932.1:n.1780+67C>T
XR_931372.1:n.179-3440G>A
XR_931373.1:n.318+2901G>A
XR_931374.1:n.117+1058G>A
NM_000834.4:c.1780+67C>T	NP_000825.2:n.1780+67C>T
XM_011520628.2:c.1780+67C>T	XP_011518930.1:n.1780+67C>T
XM_011520629.2:c.1780+67C>T	XP_011518931.1:n.1780+67C>T
XM_017019219.2:c.1780+67C>T	XP_016874708.1:n.1780+67C>T
XR_001749013.1:n.599+1058G>A
XR_931372.2:n.316-3440G>A
XR_931373.2:n.457+2901G>A
NM_000834.5:c.1780+67C>T MANE Select	NP_000825.2:n.1780+67C>T