Canonical Allele Identifier: CA603495897

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1164431928
• gnomAD v2: 12-14018706-C-A
• gnomAD v4: 12-13865772-C-A
• MyVariant Identifiers: chr12:g.14018706C>A (hg19) ; chr12:g.13865772C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865772C>A , CM000674.2:g.13865772C>A	GRCh38
NC_000012.11:g.14018706C>A , CM000674.1:g.14018706C>A	GRCh37
NC_000012.10:g.13909973C>A	NCBI36
NG_031854.1:g.119317G>T
NG_031854.2:g.121241G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+26G>T MANE Select	ENSP00000477455.1:n.411+26G>T
ENST00000630791.2:c.411+26G>T	ENSP00000486677.2:n.411+26G>T
ENST00000609686.3:c.411+26G>T	ENSP00000477455.1:n.411+26G>T
NM_000834.3:c.411+26G>T	NP_000825.2:n.411+26G>T
XM_011520628.1:c.411+26G>T	XP_011518930.1:n.411+26G>T
XM_011520629.1:c.411+26G>T	XP_011518931.1:n.411+26G>T
XM_011520630.1:c.411+26G>T	XP_011518932.1:n.411+26G>T
NM_000834.4:c.411+26G>T	NP_000825.2:n.411+26G>T
XM_011520628.2:c.411+26G>T	XP_011518930.1:n.411+26G>T
XM_011520629.2:c.411+26G>T	XP_011518931.1:n.411+26G>T
XM_017019219.2:c.411+26G>T	XP_016874708.1:n.411+26G>T
NM_000834.5:c.411+26G>T MANE Select	NP_000825.2:n.411+26G>T