Canonical Allele Identifier: CA685631823

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1171254933
• gnomAD v4: 12-13615696-CAAAA-C
• MyVariant Identifiers: chr12:g.13768631_13768634del (hg19) ; chr12:g.13615697_13615700del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615699_13615702del , CM000674.2:g.13615699_13615702del	GRCh38
NC_000012.11:g.13768633_13768636del , CM000674.1:g.13768633_13768636del	GRCh37
NC_000012.10:g.13659900_13659903del	NCBI36
NG_031854.1:g.369389_369392del
NG_031854.2:g.371313_371316del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-36_1329-33del MANE Select	ENSP00000477455.1:n.1329-36_1329-33del
ENST00000630791.2:c.1329-36_1329-33del	ENSP00000486677.2:n.1329-36_1329-33del
ENST00000609686.3:c.1329-36_1329-33del	ENSP00000477455.1:n.1329-36_1329-33del
NM_000834.3:c.1329-36_1329-33del	NP_000825.2:n.1329-36_1329-33del
XM_011520628.1:c.1329-36_1329-33del	XP_011518930.1:n.1329-36_1329-33del
XM_011520629.1:c.1329-36_1329-33del	XP_011518931.1:n.1329-36_1329-33del
XM_011520630.1:c.1329-36_1329-33del	XP_011518932.1:n.1329-36_1329-33del
XR_931372.1:n.307+473_307+476del
XR_931373.1:n.447+473_447+476del
XR_931374.1:n.246+473_246+476del
NM_000834.4:c.1329-36_1329-33del	NP_000825.2:n.1329-36_1329-33del
XM_011520628.2:c.1329-36_1329-33del	XP_011518930.1:n.1329-36_1329-33del
XM_011520629.2:c.1329-36_1329-33del	XP_011518931.1:n.1329-36_1329-33del
XM_017019219.2:c.1329-36_1329-33del	XP_016874708.1:n.1329-36_1329-33del
XR_001749013.1:n.728+473_728+476del
XR_931372.2:n.444+473_444+476del
XR_931373.2:n.586+473_586+476del
NM_000834.5:c.1329-36_1329-33del MANE Select	NP_000825.2:n.1329-36_1329-33del