Canonical Allele Identifier: CA2017462712

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949417221

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13614995G>A , CM000674.2:g.13614995G>A	GRCh38
NC_000012.11:g.13767929G>A , CM000674.1:g.13767929G>A	GRCh37
NC_000012.10:g.13659196G>A	NCBI36
NG_031854.1:g.370094C>T
NG_031854.2:g.372018C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+119C>T MANE Select	ENSP00000477455.1:n.1654+119C>T
ENST00000609686.3:c.1654+119C>T	ENSP00000477455.1:n.1654+119C>T
NM_000834.3:c.1654+119C>T	NP_000825.2:n.1654+119C>T
XM_011520628.1:c.1654+119C>T	XP_011518930.1:n.1654+119C>T
XM_011520629.1:c.1654+119C>T	XP_011518931.1:n.1654+119C>T
XM_011520630.1:c.1654+119C>T	XP_011518932.1:n.1654+119C>T
XR_931372.1:n.179-103G>A
XR_931373.1:n.319-103G>A
XR_931374.1:n.118-103G>A
NM_000834.4:c.1654+119C>T	NP_000825.2:n.1654+119C>T
XM_011520628.2:c.1654+119C>T	XP_011518930.1:n.1654+119C>T
XM_011520629.2:c.1654+119C>T	XP_011518931.1:n.1654+119C>T
XM_017019219.2:c.1654+119C>T	XP_016874708.1:n.1654+119C>T
XR_001749013.1:n.600-103G>A
XR_931372.2:n.316-103G>A
XR_931373.2:n.458-103G>A
NM_000834.5:c.1654+119C>T MANE Select	NP_000825.2:n.1654+119C>T