Canonical Allele Identifier: CA2245937985
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1167069326

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668119G>C , CM000679.2:g.7668119G>C GRCh38
NC_000017.10:g.7571437G>C , CM000679.1:g.7571437G>C GRCh37
NC_000017.9:g.7512162G>C NCBI36
NG_017013.2:g.24432C>G , LRG_321:g.24432C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1875C>G ENSP00000352610.4:n.994-1875C>G
ENST00000413465.6:c.782+6062C>G ENSP00000410739.2:n.782+6062C>G
ENST00000635293.1:c.984-694C>G ENSP00000488924.1:n.984-694C>G