Canonical Allele Identifier: CA2617718305
Gene: GRIN2B HGNC NCBI

Linked Data

gnomAD v4: 12-13562395-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562395G>T , CM000674.2:g.13562395G>T GRCh38
NC_000012.11:g.13715329G>T , CM000674.1:g.13715329G>T GRCh37
NC_000012.10:g.13606596G>T NCBI36
NG_031854.1:g.422694C>A
NG_031854.2:g.424618C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*388C>A MANE Select ENSP00000477455.1:n.*388C>A
ENST00000637214.1:c.69+46208C>A ENSP00000489997.1:n.69+46208C>A
ENST00000609686.3:c.*388C>A ENSP00000477455.1:n.*388C>A
NM_000834.3:c.*388C>A NP_000825.2:n.*388C>A
XM_005253351.2:c.*388C>A XP_005253408.1:n.*388C>A
XM_011520628.1:c.*388C>A XP_011518930.1:n.*388C>A
XM_011520629.1:c.*388C>A XP_011518931.1:n.*388C>A
XM_011520630.1:c.*388C>A XP_011518932.1:n.*388C>A
NM_000834.4:c.*388C>A NP_000825.2:n.*388C>A
XM_005253351.3:c.*388C>A XP_005253408.1:n.*388C>A
XM_011520628.2:c.*388C>A XP_011518930.1:n.*388C>A
XM_011520629.2:c.*388C>A XP_011518931.1:n.*388C>A
XM_017019219.2:c.*388C>A XP_016874708.1:n.*388C>A
NM_000834.5:c.*388C>A MANE Select NP_000825.2:n.*388C>A
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