Canonical Allele Identifier: CA2617718382
Gene: GRIN2B HGNC NCBI

Linked Data

gnomAD v4: 12-13562481-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562481G>T , CM000674.2:g.13562481G>T GRCh38
NC_000012.11:g.13715415G>T , CM000674.1:g.13715415G>T GRCh37
NC_000012.10:g.13606682G>T NCBI36
NG_031854.1:g.422608C>A
NG_031854.2:g.424532C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*302C>A MANE Select ENSP00000477455.1:n.*302C>A
ENST00000637214.1:c.69+46122C>A ENSP00000489997.1:n.69+46122C>A
ENST00000609686.3:c.*302C>A ENSP00000477455.1:n.*302C>A
NM_000834.3:c.*302C>A NP_000825.2:n.*302C>A
XM_005253351.2:c.*302C>A XP_005253408.1:n.*302C>A
XM_011520628.1:c.*302C>A XP_011518930.1:n.*302C>A
XM_011520629.1:c.*302C>A XP_011518931.1:n.*302C>A
XM_011520630.1:c.*302C>A XP_011518932.1:n.*302C>A
NM_000834.4:c.*302C>A NP_000825.2:n.*302C>A
XM_005253351.3:c.*302C>A XP_005253408.1:n.*302C>A
XM_011520628.2:c.*302C>A XP_011518930.1:n.*302C>A
XM_011520629.2:c.*302C>A XP_011518931.1:n.*302C>A
XM_017019219.2:c.*302C>A XP_016874708.1:n.*302C>A
NM_000834.5:c.*302C>A MANE Select NP_000825.2:n.*302C>A
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