Canonical Allele Identifier: CA233135263
Gene: GRIN2B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13566469G>C , CM000674.2:g.13566469G>C GRCh38
NC_000012.11:g.13719403G>C , CM000674.1:g.13719403G>C GRCh37
NC_000012.10:g.13610670G>C NCBI36
NG_031854.1:g.418620C>G
NG_031854.2:g.420544C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.2598+556C>G MANE Select ENSP00000477455.1:n.2598+556C>G
ENST00000637214.1:c.69+42134C>G ENSP00000489997.1:n.69+42134C>G
ENST00000609686.3:c.2598+556C>G ENSP00000477455.1:n.2598+556C>G
ENST00000628166.1:n.858+556C>G
NM_000834.3:c.2598+556C>G NP_000825.2:n.2598+556C>G
XM_005253351.2:c.384+556C>G XP_005253408.1:n.384+556C>G
XM_011520628.1:c.2598+556C>G XP_011518930.1:n.2598+556C>G
XM_011520629.1:c.2598+556C>G XP_011518931.1:n.2598+556C>G
XM_011520630.1:c.2598+556C>G XP_011518932.1:n.2598+556C>G
NM_000834.4:c.2598+556C>G NP_000825.2:n.2598+556C>G
XM_005253351.3:c.384+556C>G XP_005253408.1:n.384+556C>G
XM_011520628.2:c.2598+556C>G XP_011518930.1:n.2598+556C>G
XM_011520629.2:c.2598+556C>G XP_011518931.1:n.2598+556C>G
XM_017019219.2:c.2598+556C>G XP_016874708.1:n.2598+556C>G
NM_000834.5:c.2598+556C>G MANE Select NP_000825.2:n.2598+556C>G
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