Canonical Allele Identifier: CA2617717661

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13561170-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561170T>G , CM000674.2:g.13561170T>G	GRCh38
NC_000012.11:g.13714104T>G , CM000674.1:g.13714104T>G	GRCh37
NC_000012.10:g.13605371T>G	NCBI36
NG_031854.1:g.423919A>C
NG_031854.2:g.425843A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*1613A>C MANE Select	ENSP00000477455.1:n.*1613A>C
ENST00000637214.1:c.69+47433A>C	ENSP00000489997.1:n.69+47433A>C
ENST00000609686.3:c.*1613A>C	ENSP00000477455.1:n.*1613A>C
XM_005253351.2:c.*1613A>C	XP_005253408.1:n.*1613A>C
XM_011520628.1:c.*1613A>C	XP_011518930.1:n.*1613A>C
XM_011520629.1:c.*1613A>C	XP_011518931.1:n.*1613A>C
XM_011520630.1:c.*1613A>C	XP_011518932.1:n.*1613A>C
NM_000834.4:c.*1613A>C	NP_000825.2:n.*1613A>C
XM_005253351.3:c.*1613A>C	XP_005253408.1:n.*1613A>C
XM_011520628.2:c.*1613A>C	XP_011518930.1:n.*1613A>C
XM_011520629.2:c.*1613A>C	XP_011518931.1:n.*1613A>C
XM_017019219.2:c.*1613A>C	XP_016874708.1:n.*1613A>C
NM_000834.5:c.*1613A>C MANE Select	NP_000825.2:n.*1613A>C