Canonical Allele Identifier: CA2617752536

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13608591-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608591T>G , CM000674.2:g.13608591T>G	GRCh38
NC_000012.11:g.13761525T>G , CM000674.1:g.13761525T>G	GRCh37
NC_000012.10:g.13652792T>G	NCBI36
NG_031854.1:g.376498A>C
NG_031854.2:g.378422A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2010+12A>C MANE Select	ENSP00000477455.1:n.2010+12A>C
ENST00000628166.2:n.270+12A>C
ENST00000637214.1:c.69+12A>C	ENSP00000489997.1:n.69+12A>C
ENST00000609686.3:c.2010+12A>C	ENSP00000477455.1:n.2010+12A>C
ENST00000628166.1:n.270+12A>C
NM_000834.3:c.2010+12A>C	NP_000825.2:n.2010+12A>C
XM_005253351.2:c.-44+12A>C	XP_005253408.1:n.-44+12A>C
XM_011520628.1:c.2010+12A>C	XP_011518930.1:n.2010+12A>C
XM_011520629.1:c.2010+12A>C	XP_011518931.1:n.2010+12A>C
XM_011520630.1:c.2010+12A>C	XP_011518932.1:n.2010+12A>C
XR_931372.1:n.179-6507T>G
XR_931373.1:n.179-27T>G
NM_000834.4:c.2010+12A>C	NP_000825.2:n.2010+12A>C
XM_005253351.3:c.-44+12A>C	XP_005253408.1:n.-44+12A>C
XM_011520628.2:c.2010+12A>C	XP_011518930.1:n.2010+12A>C
XM_011520629.2:c.2010+12A>C	XP_011518931.1:n.2010+12A>C
XM_017019219.2:c.2010+12A>C	XP_016874708.1:n.2010+12A>C
XR_001749013.1:n.318-27T>G
XR_931372.2:n.316-6507T>G
XR_931373.2:n.318-27T>G
NM_000834.5:c.2010+12A>C MANE Select	NP_000825.2:n.2010+12A>C