Canonical Allele Identifier: CA384053643

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 2937751
• ClinVar RCV Id: RCV003794381
• MyVariant Identifiers: chr12:g.14018781G>A (hg19) ; chr12:g.13865847G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865847G>A , CM000674.2:g.13865847G>A	GRCh38
NC_000012.11:g.14018781G>A , CM000674.1:g.14018781G>A	GRCh37
NC_000012.10:g.13910048G>A	NCBI36
NG_031854.1:g.119242C>T
NG_031854.2:g.121166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.362C>T MANE Select	ENSP00000477455.1:p.Thr121Ile
ENST00000630791.2:c.362C>T	ENSP00000486677.2:p.Thr121Ile
ENST00000609686.3:c.362C>T	ENSP00000477455.1:p.Thr121Ile
NM_000834.3:c.362C>T	NP_000825.2:p.Thr121Ile
XM_011520628.1:c.362C>T	XP_011518930.1:p.Thr121Ile
XM_011520629.1:c.362C>T	XP_011518931.1:p.Thr121Ile
XM_011520630.1:c.362C>T	XP_011518932.1:p.Thr121Ile
NM_000834.4:c.362C>T	NP_000825.2:p.Thr121Ile
XM_011520628.2:c.362C>T	XP_011518930.1:p.Thr121Ile
XM_011520629.2:c.362C>T	XP_011518931.1:p.Thr121Ile
XM_017019219.2:c.362C>T	XP_016874708.1:p.Thr121Ile
NM_000834.5:c.362C>T MANE Select	NP_000825.2:p.Thr121Ile