Canonical Allele Identifier: CA656753372
Gene: TP53 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668063T>C , CM000679.2:g.7668063T>C GRCh38
NC_000017.10:g.7571381T>C , CM000679.1:g.7571381T>C GRCh37
NC_000017.9:g.7512106T>C NCBI36
NG_017013.2:g.24488A>G , LRG_321:g.24488A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1819A>G ENSP00000352610.4:n.994-1819A>G
ENST00000413465.6:c.783-6049A>G ENSP00000410739.2:n.783-6049A>G
ENST00000635293.1:c.984-638A>G ENSP00000488924.1:n.984-638A>G