Canonical Allele Identifier: CA2245938349
Community Standard Title: NC_000017.11:g.7668313C=
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668313C= , CM000679.2:g.7668313C= GRCh38
NC_000017.10:g.7571631C= , CM000679.1:g.7571631C= GRCh37
NC_000017.9:g.7512356C= NCBI36
NG_017013.2:g.24238G= , LRG_321:g.24238G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-2069G= ENSP00000352610.4:n.994-2069G=
ENST00000413465.6:c.782+5868G= ENSP00000410739.2:n.782+5868G=
ENST00000635293.1:c.984-888G= ENSP00000488924.1:n.984-888G=