Canonical Allele Identifier: CA2245938188
Gene: TP53 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668228C= , CM000679.2:g.7668228C= GRCh38
NC_000017.10:g.7571546C= , CM000679.1:g.7571546C= GRCh37
NC_000017.9:g.7512271C= NCBI36
NG_017013.2:g.24323G= , LRG_321:g.24323G=

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1984G= ENSP00000352610.4:n.994-1984G=
ENST00000413465.6:c.782+5953G= ENSP00000410739.2:n.782+5953G=
ENST00000635293.1:c.984-803G= ENSP00000488924.1:n.984-803G=
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