Canonical Allele Identifier: CA2245938046
Gene: TP53 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668170G= , CM000679.2:g.7668170G= GRCh38
NC_000017.10:g.7571488G= , CM000679.1:g.7571488G= GRCh37
NC_000017.9:g.7512213G= NCBI36
NG_017013.2:g.24381C= , LRG_321:g.24381C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1926C= ENSP00000352610.4:n.994-1926C=
ENST00000413465.6:c.782+6011C= ENSP00000410739.2:n.782+6011C=
ENST00000635293.1:c.984-745C= ENSP00000488924.1:n.984-745C=
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