Canonical Allele Identifier: CA384051151

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13761671T>A (hg19) ; chr12:g.13608737T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608737T>A , CM000674.2:g.13608737T>A	GRCh38
NC_000012.11:g.13761671T>A , CM000674.1:g.13761671T>A	GRCh37
NC_000012.10:g.13652938T>A	NCBI36
NG_031854.1:g.376352A>T
NG_031854.2:g.378276A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1876A>T MANE Select	ENSP00000477455.1:p.Thr626Ser
ENST00000628166.2:n.136A>T
ENST00000609686.3:c.1876A>T	ENSP00000477455.1:p.Thr626Ser
ENST00000628166.1:n.136A>T
NM_000834.3:c.1876A>T	NP_000825.2:p.Thr626Ser
XM_011520628.1:c.1876A>T	XP_011518930.1:p.Thr626Ser
XM_011520629.1:c.1876A>T	XP_011518931.1:p.Thr626Ser
XM_011520630.1:c.1876A>T	XP_011518932.1:p.Thr626Ser
XR_931372.1:n.179-6361T>A
XR_931373.1:n.298T>A
NM_000834.4:c.1876A>T	NP_000825.2:p.Thr626Ser
XM_011520628.2:c.1876A>T	XP_011518930.1:p.Thr626Ser
XM_011520629.2:c.1876A>T	XP_011518931.1:p.Thr626Ser
XM_017019219.2:c.1876A>T	XP_016874708.1:p.Thr626Ser
XR_001749013.1:n.437T>A
XR_931372.2:n.316-6361T>A
XR_931373.2:n.437T>A
NM_000834.5:c.1876A>T MANE Select	NP_000825.2:p.Thr626Ser