Canonical Allele Identifier: CA2560656293
Gene: TP53 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668218G>T , CM000679.2:g.7668218G>T GRCh38
NC_000017.10:g.7571536G>T , CM000679.1:g.7571536G>T GRCh37
NC_000017.9:g.7512261G>T NCBI36
NG_017013.2:g.24333C>A , LRG_321:g.24333C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1974C>A ENSP00000352610.4:n.994-1974C>A
ENST00000413465.6:c.782+5963C>A ENSP00000410739.2:n.782+5963C>A
ENST00000635293.1:c.984-793C>A ENSP00000488924.1:n.984-793C>A
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