Canonical Allele Identifier: CA2617757688

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13866369-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866369A>C , CM000674.2:g.13866369A>C	GRCh38
NC_000012.11:g.14019303A>C , CM000674.1:g.14019303A>C	GRCh37
NC_000012.10:g.13910570A>C	NCBI36
NG_031854.1:g.118720T>G
NG_031854.2:g.120644T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-18-143T>G MANE Select	ENSP00000477455.1:n.-18-143T>G
ENST00000630791.2:c.-18-143T>G	ENSP00000486677.2:n.-18-143T>G
ENST00000609686.3:c.-18-143T>G	ENSP00000477455.1:n.-18-143T>G
ENST00000627535.2:c.-18-143T>G	ENSP00000486411.1:n.-18-143T>G
ENST00000630791.1:c.-18-143T>G	ENSP00000486677.1:n.-18-143T>G
NM_000834.3:c.-18-143T>G	NP_000825.2:n.-18-143T>G
XM_011520628.1:c.-18-143T>G	XP_011518930.1:n.-18-143T>G
XM_011520629.1:c.-18-143T>G	XP_011518931.1:n.-18-143T>G
XM_011520630.1:c.-18-143T>G	XP_011518932.1:n.-18-143T>G
NM_000834.4:c.-18-143T>G	NP_000825.2:n.-18-143T>G
XM_011520628.2:c.-18-143T>G	XP_011518930.1:n.-18-143T>G
XM_011520629.2:c.-18-143T>G	XP_011518931.1:n.-18-143T>G
XM_017019219.2:c.-18-143T>G	XP_016874708.1:n.-18-143T>G
NM_000834.5:c.-18-143T>G MANE Select	NP_000825.2:n.-18-143T>G