Canonical Allele Identifier: CA383986011

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13563026-G-T
• MyVariant Identifiers: chr12:g.13715960G>T (hg19) ; chr12:g.13563026G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13563026G>T , CM000674.2:g.13563026G>T	GRCh38
NC_000012.11:g.13715960G>T , CM000674.1:g.13715960G>T	GRCh37
NC_000012.10:g.13607227G>T	NCBI36
NG_031854.1:g.422063C>A
NG_031854.2:g.423987C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.4212C>A MANE Select	ENSP00000477455.1:p.Tyr1404Ter
ENST00000637214.1:c.69+45577C>A	ENSP00000489997.1:n.69+45577C>A
ENST00000609686.3:c.4212C>A	ENSP00000477455.1:p.Tyr1404Ter
ENST00000628166.1:n.2472C>A
NM_000834.3:c.4212C>A	NP_000825.2:p.Tyr1404Ter
XM_005253351.2:c.1998C>A	XP_005253408.1:p.Tyr666Ter
XM_011520628.1:c.4212C>A	XP_011518930.1:p.Tyr1404Ter
XM_011520629.1:c.4212C>A	XP_011518931.1:p.Tyr1404Ter
XM_011520630.1:c.4212C>A	XP_011518932.1:p.Tyr1404Ter
NM_000834.4:c.4212C>A	NP_000825.2:p.Tyr1404Ter
XM_005253351.3:c.1998C>A	XP_005253408.1:p.Tyr666Ter
XM_011520628.2:c.4212C>A	XP_011518930.1:p.Tyr1404Ter
XM_011520629.2:c.4212C>A	XP_011518931.1:p.Tyr1404Ter
XM_017019219.2:c.4212C>A	XP_016874708.1:p.Tyr1404Ter
NM_000834.5:c.4212C>A MANE Select	NP_000825.2:p.Tyr1404Ter