Canonical Allele Identifier: CA2245938329
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668304C= , CM000679.2:g.7668304C= GRCh38
NC_000017.10:g.7571622C= , CM000679.1:g.7571622C= GRCh37
NC_000017.9:g.7512347C= NCBI36
NG_017013.2:g.24247G= , LRG_321:g.24247G=

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2060G= ENSP00000352610.4:n.994-2060G=
ENST00000413465.6:c.782+5877G= ENSP00000410739.2:n.782+5877G=
ENST00000635293.1:c.984-879G= ENSP00000488924.1:n.984-879G=