Canonical Allele Identifier: CA6461155

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 1092676
• ClinVar RCV Id: RCV001412562
• dbSNP Id: rs767875110
• ExAC: 12:13761624 G / T
• gnomAD v2: 12-13761624-G-T
• gnomAD v3: 12-13608690-G-T
• gnomAD v4: 12-13608690-G-T
• MyVariant Identifiers: chr12:g.13761624G>T (hg19) ; chr12:g.13608690G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608690G>T , CM000674.2:g.13608690G>T	GRCh38
NC_000012.11:g.13761624G>T , CM000674.1:g.13761624G>T	GRCh37
NC_000012.10:g.13652891G>T	NCBI36
NG_031854.1:g.376399C>A
NG_031854.2:g.378323C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1923C>A MANE Select	ENSP00000477455.1:p.Ile641=
ENST00000628166.2:n.183C>A
ENST00000609686.3:c.1923C>A	ENSP00000477455.1:p.Ile641=
ENST00000628166.1:n.183C>A
NM_000834.3:c.1923C>A	NP_000825.2:p.Ile641=
XM_011520628.1:c.1923C>A	XP_011518930.1:p.Ile641=
XM_011520629.1:c.1923C>A	XP_011518931.1:p.Ile641=
XM_011520630.1:c.1923C>A	XP_011518932.1:p.Ile641=
XR_931372.1:n.179-6408G>T
XR_931373.1:n.251G>T
NM_000834.4:c.1923C>A	NP_000825.2:p.Ile641=
XM_011520628.2:c.1923C>A	XP_011518930.1:p.Ile641=
XM_011520629.2:c.1923C>A	XP_011518931.1:p.Ile641=
XM_017019219.2:c.1923C>A	XP_016874708.1:p.Ile641=
XR_001749013.1:n.390G>T
XR_931372.2:n.316-6408G>T
XR_931373.2:n.390G>T
NM_000834.5:c.1923C>A MANE Select	NP_000825.2:p.Ile641=