Canonical Allele Identifier: CA2617757586

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13865791-T-G

Genomic Alleles

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

Transcript Alleles

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