Canonical Allele Identifier: CA384050993

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13761612G>T (hg19) ; chr12:g.13608678G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608678G>T , CM000674.2:g.13608678G>T	GRCh38
NC_000012.11:g.13761612G>T , CM000674.1:g.13761612G>T	GRCh37
NC_000012.10:g.13652879G>T	NCBI36
NG_031854.1:g.376411C>A
NG_031854.2:g.378335C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1935C>A MANE Select	ENSP00000477455.1:p.Ser645Arg
ENST00000628166.2:n.195C>A
ENST00000609686.3:c.1935C>A	ENSP00000477455.1:p.Ser645Arg
ENST00000628166.1:n.195C>A
NM_000834.3:c.1935C>A	NP_000825.2:p.Ser645Arg
XM_011520628.1:c.1935C>A	XP_011518930.1:p.Ser645Arg
XM_011520629.1:c.1935C>A	XP_011518931.1:p.Ser645Arg
XM_011520630.1:c.1935C>A	XP_011518932.1:p.Ser645Arg
XR_931372.1:n.179-6420G>T
XR_931373.1:n.239G>T
NM_000834.4:c.1935C>A	NP_000825.2:p.Ser645Arg
XM_005253351.3:c.-119C>A	XP_005253408.1:n.-119C>A
XM_011520628.2:c.1935C>A	XP_011518930.1:p.Ser645Arg
XM_011520629.2:c.1935C>A	XP_011518931.1:p.Ser645Arg
XM_017019219.2:c.1935C>A	XP_016874708.1:p.Ser645Arg
XR_001749013.1:n.378G>T
XR_931372.2:n.316-6420G>T
XR_931373.2:n.378G>T
NM_000834.5:c.1935C>A MANE Select	NP_000825.2:p.Ser645Arg