Canonical Allele Identifier: CA2245938229
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1597342318

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668243G>A , CM000679.2:g.7668243G>A GRCh38
NC_000017.10:g.7571561G>A , CM000679.1:g.7571561G>A GRCh37
NC_000017.9:g.7512286G>A NCBI36
NG_017013.2:g.24308C>T , LRG_321:g.24308C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1999C>T ENSP00000352610.4:n.994-1999C>T
ENST00000413465.6:c.782+5938C>T ENSP00000410739.2:n.782+5938C>T
ENST00000635293.1:c.984-818C>T ENSP00000488924.1:n.984-818C>T