Canonical Allele Identifier: CA685630914

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1182106568
• gnomAD v3: 12-13615110-T-TTACC
• gnomAD v4: 12-13615110-T-TTACC
• MyVariant Identifiers: chr12:g.13768044_13768045insTACC (hg19) ; chr12:g.13615110_13615111insTACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615113_13615116dup , CM000674.2:g.13615113_13615116dup	GRCh38
NC_000012.11:g.13768047_13768050dup , CM000674.1:g.13768047_13768050dup	GRCh37
NC_000012.10:g.13659314_13659317dup	NCBI36
NG_031854.1:g.369975_369978dup
NG_031854.2:g.371899_371902dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654_1654+3dup
ENST00000609686.3:c.1654_1654+3dup
NM_000834.3:c.1654_1654+3dup
XM_011520628.1:c.1654_1654+3dup
XM_011520629.1:c.1654_1654+3dup
XM_011520630.1:c.1654_1654+3dup
XR_931372.1:n.194_197dup
XR_931373.1:n.334_337dup
XR_931374.1:n.133_136dup
NM_000834.4:c.1654_1654+3dup
XM_011520628.2:c.1654_1654+3dup
XM_011520629.2:c.1654_1654+3dup
XM_017019219.2:c.1654_1654+3dup
XR_001749013.1:n.615_618dup
XR_931372.2:n.331_334dup
XR_931373.2:n.473_476dup
NM_000834.5:c.1654_1654+3dup