Canonical Allele Identifier: CA2617750984

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13614962-TTTTGAAGTCCCCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13614963_13614976del , CM000674.2:g.13614963_13614976del	GRCh38
NC_000012.11:g.13767897_13767910del , CM000674.1:g.13767897_13767910del	GRCh37
NC_000012.10:g.13659164_13659177del	NCBI36
NG_031854.1:g.370113_370126del
NG_031854.2:g.372037_372050del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+138_1654+151del MANE Select	ENSP00000477455.1:n.1654+138_1654+151del
ENST00000609686.3:c.1654+138_1654+151del	ENSP00000477455.1:n.1654+138_1654+151del
NM_000834.3:c.1654+138_1654+151del	NP_000825.2:n.1654+138_1654+151del
XM_011520628.1:c.1654+138_1654+151del	XP_011518930.1:n.1654+138_1654+151del
XM_011520629.1:c.1654+138_1654+151del	XP_011518931.1:n.1654+138_1654+151del
XM_011520630.1:c.1654+138_1654+151del	XP_011518932.1:n.1654+138_1654+151del
XR_931372.1:n.179-135_179-122del
XR_931373.1:n.319-135_319-122del
XR_931374.1:n.118-135_118-122del
NM_000834.4:c.1654+138_1654+151del	NP_000825.2:n.1654+138_1654+151del
XM_011520628.2:c.1654+138_1654+151del	XP_011518930.1:n.1654+138_1654+151del
XM_011520629.2:c.1654+138_1654+151del	XP_011518931.1:n.1654+138_1654+151del
XM_017019219.2:c.1654+138_1654+151del	XP_016874708.1:n.1654+138_1654+151del
XR_001749013.1:n.600-135_600-122del
XR_931372.2:n.316-135_316-122del
XR_931373.2:n.458-135_458-122del
NM_000834.5:c.1654+138_1654+151del MANE Select	NP_000825.2:n.1654+138_1654+151del