Canonical Allele Identifier: CA384052017

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768203T>C (hg19) ; chr12:g.13615269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615269T>C , CM000674.2:g.13615269T>C	GRCh38
NC_000012.11:g.13768203T>C , CM000674.1:g.13768203T>C	GRCh37
NC_000012.10:g.13659470T>C	NCBI36
NG_031854.1:g.369820A>G
NG_031854.2:g.371744A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-2A>G MANE Select	ENSP00000477455.1:n.1501-2A>G
ENST00000609686.3:c.1501-2A>G	ENSP00000477455.1:n.1501-2A>G
NM_000834.3:c.1501-2A>G	NP_000825.2:n.1501-2A>G
XM_011520628.1:c.1501-2A>G	XP_011518930.1:n.1501-2A>G
XM_011520629.1:c.1501-2A>G	XP_011518931.1:n.1501-2A>G
XM_011520630.1:c.1501-2A>G	XP_011518932.1:n.1501-2A>G
XR_931372.1:n.307+43T>C
XR_931373.1:n.447+43T>C
XR_931374.1:n.246+43T>C
NM_000834.4:c.1501-2A>G	NP_000825.2:n.1501-2A>G
XM_011520628.2:c.1501-2A>G	XP_011518930.1:n.1501-2A>G
XM_011520629.2:c.1501-2A>G	XP_011518931.1:n.1501-2A>G
XM_017019219.2:c.1501-2A>G	XP_016874708.1:n.1501-2A>G
XR_001749013.1:n.728+43T>C
XR_931372.2:n.444+43T>C
XR_931373.2:n.586+43T>C
NM_000834.5:c.1501-2A>G MANE Select	NP_000825.2:n.1501-2A>G