Canonical Allele Identifier: CA2245938387
Gene: TP53 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668345C= , CM000679.2:g.7668345C= GRCh38
NC_000017.10:g.7571663C= , CM000679.1:g.7571663C= GRCh37
NC_000017.9:g.7512388C= NCBI36
NG_017013.2:g.24206G= , LRG_321:g.24206G=

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2101G= ENSP00000352610.4:n.994-2101G=
ENST00000413465.6:c.782+5836G= ENSP00000410739.2:n.782+5836G=
ENST00000635293.1:c.984-920G= ENSP00000488924.1:n.984-920G=
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