Canonical Allele Identifier: CA2245938348
Community Standard Title: NC_000017.11:g.7668312C=
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668312C= , CM000679.2:g.7668312C= GRCh38
NC_000017.10:g.7571630C= , CM000679.1:g.7571630C= GRCh37
NC_000017.9:g.7512355C= NCBI36
NG_017013.2:g.24239G= , LRG_321:g.24239G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-2068G= ENSP00000352610.4:n.994-2068G=
ENST00000413465.6:c.782+5869G= ENSP00000410739.2:n.782+5869G=
ENST00000635293.1:c.984-887G= ENSP00000488924.1:n.984-887G=