Canonical Allele Identifier: CA2017462770

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949418251

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615055_13615057del , CM000674.2:g.13615055_13615057del	GRCh38
NC_000012.11:g.13767989_13767991del , CM000674.1:g.13767989_13767991del	GRCh37
NC_000012.10:g.13659256_13659258del	NCBI36
NG_031854.1:g.370032_370034del
NG_031854.2:g.371956_371958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+57_1654+59del MANE Select	ENSP00000477455.1:n.1654+57_1654+59del
ENST00000609686.3:c.1654+57_1654+59del	ENSP00000477455.1:n.1654+57_1654+59del
NM_000834.3:c.1654+57_1654+59del	NP_000825.2:n.1654+57_1654+59del
XM_011520628.1:c.1654+57_1654+59del	XP_011518930.1:n.1654+57_1654+59del
XM_011520629.1:c.1654+57_1654+59del	XP_011518931.1:n.1654+57_1654+59del
XM_011520630.1:c.1654+57_1654+59del	XP_011518932.1:n.1654+57_1654+59del
XR_931372.1:n.179-43_179-41del
XR_931373.1:n.319-43_319-41del
XR_931374.1:n.118-43_118-41del
NM_000834.4:c.1654+57_1654+59del	NP_000825.2:n.1654+57_1654+59del
XM_011520628.2:c.1654+57_1654+59del	XP_011518930.1:n.1654+57_1654+59del
XM_011520629.2:c.1654+57_1654+59del	XP_011518931.1:n.1654+57_1654+59del
XM_017019219.2:c.1654+57_1654+59del	XP_016874708.1:n.1654+57_1654+59del
XR_001749013.1:n.600-43_600-41del
XR_931372.2:n.316-43_316-41del
XR_931373.2:n.458-43_458-41del
NM_000834.5:c.1654+57_1654+59del MANE Select	NP_000825.2:n.1654+57_1654+59del