Canonical Allele Identifier: CA2245937995
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668134G= , CM000679.2:g.7668134G= GRCh38
NC_000017.10:g.7571452G= , CM000679.1:g.7571452G= GRCh37
NC_000017.9:g.7512177G= NCBI36
NG_017013.2:g.24417C= , LRG_321:g.24417C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1890C= ENSP00000352610.4:n.994-1890C=
ENST00000413465.6:c.782+6047C= ENSP00000410739.2:n.782+6047C=
ENST00000635293.1:c.984-709C= ENSP00000488924.1:n.984-709C=