Canonical Allele Identifier: CA2245938157
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668223A= , CM000679.2:g.7668223A= GRCh38
NC_000017.10:g.7571541A= , CM000679.1:g.7571541A= GRCh37
NC_000017.9:g.7512266A= NCBI36
NG_017013.2:g.24328T= , LRG_321:g.24328T=

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1979T= ENSP00000352610.4:n.994-1979T=
ENST00000413465.6:c.782+5958T= ENSP00000410739.2:n.782+5958T=
ENST00000635293.1:c.984-798T= ENSP00000488924.1:n.984-798T=