Canonical Allele Identifier: CA2617758466
Gene: GRIN2B HGNC NCBI

Linked Data

gnomAD v4: 12-13981834-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981834C>A , CM000674.2:g.13981834C>A GRCh38
NC_000012.11:g.14134768C>A , CM000674.1:g.14134768C>A GRCh37
NC_000012.10:g.14026035C>A NCBI36
NG_031854.1:g.3255G>T
NG_031854.2:g.5179G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000630791.2:c.-683+82G>T ENSP00000486677.2:n.-683+82G>T
ENST00000627535.2:c.-448+82G>T ENSP00000486411.1:n.-448+82G>T
ENST00000630791.1:c.-683+82G>T ENSP00000486677.1:n.-683+82G>T
XM_011520629.1:c.-683+82G>T XP_011518931.1:n.-683+82G>T
XM_011520628.2:c.-940G>T XP_011518930.1:n.-940G>T
XM_011520629.2:c.-683+82G>T XP_011518931.1:n.-683+82G>T
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