Canonical Allele Identifier: CA384052364

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768571G>T (hg19) ; chr12:g.13615637G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615637G>T , CM000674.2:g.13615637G>T	GRCh38
NC_000012.11:g.13768571G>T , CM000674.1:g.13768571G>T	GRCh37
NC_000012.10:g.13659838G>T	NCBI36
NG_031854.1:g.369452C>A
NG_031854.2:g.371376C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1356C>A MANE Select	ENSP00000477455.1:p.Tyr452Ter
ENST00000630791.2:c.1356C>A	ENSP00000486677.2:p.Tyr452Ter
ENST00000609686.3:c.1356C>A	ENSP00000477455.1:p.Tyr452Ter
NM_000834.3:c.1356C>A	NP_000825.2:p.Tyr452Ter
XM_011520628.1:c.1356C>A	XP_011518930.1:p.Tyr452Ter
XM_011520629.1:c.1356C>A	XP_011518931.1:p.Tyr452Ter
XM_011520630.1:c.1356C>A	XP_011518932.1:p.Tyr452Ter
XR_931372.1:n.307+411G>T
XR_931373.1:n.447+411G>T
XR_931374.1:n.246+411G>T
NM_000834.4:c.1356C>A	NP_000825.2:p.Tyr452Ter
XM_011520628.2:c.1356C>A	XP_011518930.1:p.Tyr452Ter
XM_011520629.2:c.1356C>A	XP_011518931.1:p.Tyr452Ter
XM_017019219.2:c.1356C>A	XP_016874708.1:p.Tyr452Ter
XR_001749013.1:n.728+411G>T
XR_931372.2:n.444+411G>T
XR_931373.2:n.586+411G>T
NM_000834.5:c.1356C>A MANE Select	NP_000825.2:p.Tyr452Ter