Canonical Allele Identifier: CA2245938120
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668191G= , CM000679.2:g.7668191G= GRCh38
NC_000017.10:g.7571509G= , CM000679.1:g.7571509G= GRCh37
NC_000017.9:g.7512234G= NCBI36
NG_017013.2:g.24360C= , LRG_321:g.24360C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1947C= ENSP00000352610.4:n.994-1947C=
ENST00000413465.6:c.782+5990C= ENSP00000410739.2:n.782+5990C=
ENST00000635293.1:c.984-766C= ENSP00000488924.1:n.984-766C=