Canonical Allele Identifier: CA478772844

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768175T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615241T>G , CM000674.2:g.13615241T>G	GRCh38
NC_000012.11:g.13768175T>G , CM000674.1:g.13768175T>G	GRCh37
NC_000012.10:g.13659442T>G	NCBI36
NG_031854.1:g.369848A>C
NG_031854.2:g.371772A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1527A>C MANE Select	ENSP00000477455.1:p.Ala509=
ENST00000609686.3:c.1527A>C	ENSP00000477455.1:p.Ala509=
NM_000834.3:c.1527A>C	NP_000825.2:p.Ala509=
XM_011520628.1:c.1527A>C	XP_011518930.1:p.Ala509=
XM_011520629.1:c.1527A>C	XP_011518931.1:p.Ala509=
XM_011520630.1:c.1527A>C	XP_011518932.1:p.Ala509=
XR_931372.1:n.307+15T>G
XR_931373.1:n.447+15T>G
XR_931374.1:n.246+15T>G
NM_000834.4:c.1527A>C	NP_000825.2:p.Ala509=
XM_011520628.2:c.1527A>C	XP_011518930.1:p.Ala509=
XM_011520629.2:c.1527A>C	XP_011518931.1:p.Ala509=
XM_017019219.2:c.1527A>C	XP_016874708.1:p.Ala509=
XR_001749013.1:n.728+15T>G
XR_931372.2:n.444+15T>G
XR_931373.2:n.586+15T>G
NM_000834.5:c.1527A>C MANE Select	NP_000825.2:p.Ala509=