Canonical Allele Identifier: CA775165310
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1435378249
gnomAD v3: 17-7668117-G-A
gnomAD v4: 17-7668117-G-A
MyVariant Identifiers: chr17:g.7571435G>A (hg19) chr17:g.7668117G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668117G>A , CM000679.2:g.7668117G>A GRCh38
NC_000017.10:g.7571435G>A , CM000679.1:g.7571435G>A GRCh37
NC_000017.9:g.7512160G>A NCBI36
NG_017013.2:g.24434C>T , LRG_321:g.24434C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1873C>T ENSP00000352610.4:n.994-1873C>T
ENST00000413465.6:c.782+6064C>T ENSP00000410739.2:n.782+6064C>T
ENST00000635293.1:c.984-692C>T ENSP00000488924.1:n.984-692C>T
Search 100 bp 5'
Search 100 bp 3'