Canonical Allele Identifier: CA685661407
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1491431632
gnomAD v3: 12-13562302-T-TTTCCTTTCACAAGC
gnomAD v4: 12-13562302-T-TTTCCTTTCACAAGC
MyVariant Identifiers: chr12:g.13715236_13715237insTTCCTTTCACAAGC (hg19) chr12:g.13562302_13562303insTTCCTTTCACAAGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562303_13562316dup , CM000674.2:g.13562303_13562316dup GRCh38
NC_000012.11:g.13715237_13715250dup , CM000674.1:g.13715237_13715250dup GRCh37
NC_000012.10:g.13606504_13606517dup NCBI36
NG_031854.1:g.422773_422786dup
NG_031854.2:g.424697_424710dup

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*467_*480dup MANE Select ENSP00000477455.1:n.*467_*480dup
ENST00000637214.1:c.69+46287_69+46300dup ENSP00000489997.1:n.69+46287_69+46300dup
ENST00000609686.3:c.*467_*480dup ENSP00000477455.1:n.*467_*480dup
NM_000834.3:c.*467_*480dup NP_000825.2:n.*467_*480dup
XM_005253351.2:c.*467_*480dup XP_005253408.1:n.*467_*480dup
XM_011520628.1:c.*467_*480dup XP_011518930.1:n.*467_*480dup
XM_011520629.1:c.*467_*480dup XP_011518931.1:n.*467_*480dup
XM_011520630.1:c.*467_*480dup XP_011518932.1:n.*467_*480dup
NM_000834.4:c.*467_*480dup NP_000825.2:n.*467_*480dup
XM_005253351.3:c.*467_*480dup XP_005253408.1:n.*467_*480dup
XM_011520628.2:c.*467_*480dup XP_011518930.1:n.*467_*480dup
XM_011520629.2:c.*467_*480dup XP_011518931.1:n.*467_*480dup
XM_017019219.2:c.*467_*480dup XP_016874708.1:n.*467_*480dup
NM_000834.5:c.*467_*480dup MANE Select NP_000825.2:n.*467_*480dup
Search 100 bp 5'
Search 100 bp 3'