Canonical Allele Identifier: CA2245937949
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668091C= , CM000679.2:g.7668091C= GRCh38
NC_000017.10:g.7571409C= , CM000679.1:g.7571409C= GRCh37
NC_000017.9:g.7512134C= NCBI36
NG_017013.2:g.24460G= , LRG_321:g.24460G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1847G= ENSP00000352610.4:n.994-1847G=
ENST00000413465.6:c.783-6077G= ENSP00000410739.2:n.783-6077G=
ENST00000635293.1:c.984-666G= ENSP00000488924.1:n.984-666G=