Canonical Allele Identifier: CA2245938062
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs930666451

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668173G>C , CM000679.2:g.7668173G>C GRCh38
NC_000017.10:g.7571491G>C , CM000679.1:g.7571491G>C GRCh37
NC_000017.9:g.7512216G>C NCBI36
NG_017013.2:g.24378C>G , LRG_321:g.24378C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1929C>G ENSP00000352610.4:n.994-1929C>G
ENST00000413465.6:c.782+6008C>G ENSP00000410739.2:n.782+6008C>G
ENST00000635293.1:c.984-748C>G ENSP00000488924.1:n.984-748C>G