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Canonical Allele Identifier: Get Identifier
Gene: GRIN2B HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
ENSP00000486677.2:p.Cys456Tyr
ENST00000630791.2:c.[1367G>A;1371C=]

ENST00000630791.2:c.[1367G>A;1371C>T]

ENST00000630791.2:c.[1367G>A;1372A=]

ENST00000630791.2:c.[1367G>A;1374G>A]

ENST00000630791.2:c.[1367G>A;1377G>A]

ENST00000630791.2:c.[1367G>A;1377G>C]

ENST00000630791.2:c.[1367G>A;1377G=]

ENST00000630791.2:c.[1367G>A;1377G>T]

ENST00000630791.2:c.[1367G>A;1380C=]

ENST00000630791.2:c.[1367G>A;1380C>T]

ENST00000630791.2:c.[1367G>A;1381T=]

ENST00000630791.2:c.[1367G>A;1382G=]

ENST00000630791.2:c.[1367G>A;1383T>C]

ENST00000630791.2:c.[1367G>A;1383T=]

ENST00000630791.2:c.[1367G>A;1384A=]

ENST00000630791.2:c.[1367G>A;1386T>A]

ENST00000630791.2:c.[1367G>A;1386T>C]

ENST00000630791.2:c.[1367G>A;1389C=]

ENST00000630791.2:c.[1367G>A;1389C>T]