Canonical Allele Identifier: CA384050960

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13761605C>T (hg19) ; chr12:g.13608671C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608671C>T , CM000674.2:g.13608671C>T	GRCh38
NC_000012.11:g.13761605C>T , CM000674.1:g.13761605C>T	GRCh37
NC_000012.10:g.13652872C>T	NCBI36
NG_031854.1:g.376418G>A
NG_031854.2:g.378342G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1942G>A MANE Select	ENSP00000477455.1:p.Ala648Thr
ENST00000628166.2:n.202G>A
ENST00000637214.1:c.1G>A	ENSP00000489997.1:p.Ala1Thr
ENST00000609686.3:c.1942G>A	ENSP00000477455.1:p.Ala648Thr
ENST00000628166.1:n.202G>A
NM_000834.3:c.1942G>A	NP_000825.2:p.Ala648Thr
XM_005253351.2:c.-112G>A	XP_005253408.1:n.-112G>A
XM_011520628.1:c.1942G>A	XP_011518930.1:p.Ala648Thr
XM_011520629.1:c.1942G>A	XP_011518931.1:p.Ala648Thr
XM_011520630.1:c.1942G>A	XP_011518932.1:p.Ala648Thr
XR_931372.1:n.179-6427C>T
XR_931373.1:n.232C>T
NM_000834.4:c.1942G>A	NP_000825.2:p.Ala648Thr
XM_005253351.3:c.-112G>A	XP_005253408.1:n.-112G>A
XM_011520628.2:c.1942G>A	XP_011518930.1:p.Ala648Thr
XM_011520629.2:c.1942G>A	XP_011518931.1:p.Ala648Thr
XM_017019219.2:c.1942G>A	XP_016874708.1:p.Ala648Thr
XR_001749013.1:n.371C>T
XR_931372.2:n.316-6427C>T
XR_931373.2:n.371C>T
NM_000834.5:c.1942G>A MANE Select	NP_000825.2:p.Ala648Thr