Canonical Allele Identifier: CA2808381157
Gene: TP53 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668271C>G , CM000679.2:g.7668271C>G GRCh38
NC_000017.10:g.7571589C>G , CM000679.1:g.7571589C>G GRCh37
NC_000017.9:g.7512314C>G NCBI36
NG_017013.2:g.24280G>C , LRG_321:g.24280G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-2027G>C ENSP00000352610.4:n.994-2027G>C
ENST00000413465.6:c.782+5910G>C ENSP00000410739.2:n.782+5910G>C
ENST00000635293.1:c.984-846G>C ENSP00000488924.1:n.984-846G>C