Canonical Allele Identifier: CA6461073
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs760332424
ExAC: 12:13722738 G / GGGCACTTTCCCTTTCTTGAACTCACCATCTC
gnomAD v2: 12-13722738-G-GGGCACTTTCCCTTTCTTGAACTCACCATCTC
gnomAD v3: 12-13569804-G-GGGCACTTTCCCTTTCTTGAACTCACCATCTC
gnomAD v4: 12-13569804-G-GGGCACTTTCCCTTTCTTGAACTCACCATCTC
MyVariant Identifiers: chr12:g.13722738_13722739insGGCACTTTCCCTTTCTTGAACTCACCATCTC (hg19) chr12:g.13569804_13569805insGGCACTTTCCCTTTCTTGAACTCACCATCTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13569805_13569835dup , CM000674.2:g.13569805_13569835dup GRCh38
NC_000012.11:g.13722739_13722769dup , CM000674.1:g.13722739_13722769dup GRCh37
NC_000012.10:g.13614006_13614036dup NCBI36
NG_031854.1:g.415254_415284dup
NG_031854.2:g.417178_417208dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.2354_2359+25dup
ENST00000628166.2:n.614_619+25dup
ENST00000637214.1:c.69+38768_69+38798dup ENSP00000489997.1:n.69+38768_69+38798dup
ENST00000609686.3:c.2354_2359+25dup
ENST00000628166.1:n.614_619+25dup
NM_000834.3:c.2354_2359+25dup
XM_005253351.2:c.140_145+25dup
XM_011520628.1:c.2354_2359+25dup
XM_011520629.1:c.2354_2359+25dup
XM_011520630.1:c.2354_2359+25dup
NM_000834.4:c.2354_2359+25dup
XM_005253351.3:c.140_145+25dup
XM_011520628.2:c.2354_2359+25dup
XM_011520629.2:c.2354_2359+25dup
XM_017019219.2:c.2354_2359+25dup
NM_000834.5:c.2354_2359+25dup
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