Canonical Allele Identifier: CA2245937435
Community Standard Title: NC_000017.11:g.7667753T=
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7667753T= , CM000679.2:g.7667753T= GRCh38
NC_000017.10:g.7571071T= , CM000679.1:g.7571071T= GRCh37
NC_000017.9:g.7511796T= NCBI36
NG_017013.2:g.24798A= , LRG_321:g.24798A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1509A= ENSP00000352610.4:n.994-1509A=
ENST00000413465.6:c.783-5739A= ENSP00000410739.2:n.783-5739A=
ENST00000635293.1:c.984-328A= ENSP00000488924.1:n.984-328A=