Canonical Allele Identifier: CA2617757585

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13865791-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865791T>C , CM000674.2:g.13865791T>C	GRCh38
NC_000012.11:g.14018725T>C , CM000674.1:g.14018725T>C	GRCh37
NC_000012.10:g.13909992T>C	NCBI36
NG_031854.1:g.119298A>G
NG_031854.2:g.121222A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+7A>G MANE Select	ENSP00000477455.1:n.411+7A>G
ENST00000630791.2:c.411+7A>G	ENSP00000486677.2:n.411+7A>G
ENST00000609686.3:c.411+7A>G	ENSP00000477455.1:n.411+7A>G
NM_000834.3:c.411+7A>G	NP_000825.2:n.411+7A>G
XM_011520628.1:c.411+7A>G	XP_011518930.1:n.411+7A>G
XM_011520629.1:c.411+7A>G	XP_011518931.1:n.411+7A>G
XM_011520630.1:c.411+7A>G	XP_011518932.1:n.411+7A>G
NM_000834.4:c.411+7A>G	NP_000825.2:n.411+7A>G
XM_011520628.2:c.411+7A>G	XP_011518930.1:n.411+7A>G
XM_011520629.2:c.411+7A>G	XP_011518931.1:n.411+7A>G
XM_017019219.2:c.411+7A>G	XP_016874708.1:n.411+7A>G
NM_000834.5:c.411+7A>G MANE Select	NP_000825.2:n.411+7A>G