Canonical Allele Identifier: CA775165367
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1315437959
gnomAD v3: 17-7668242-T-G
gnomAD v4: 17-7668242-T-G
MyVariant Identifiers: chr17:g.7571560T>G (hg19) chr17:g.7668242T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668242T>G , CM000679.2:g.7668242T>G GRCh38
NC_000017.10:g.7571560T>G , CM000679.1:g.7571560T>G GRCh37
NC_000017.9:g.7512285T>G NCBI36
NG_017013.2:g.24309A>C , LRG_321:g.24309A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1998A>C ENSP00000352610.4:n.994-1998A>C
ENST00000413465.6:c.782+5939A>C ENSP00000410739.2:n.782+5939A>C
ENST00000635293.1:c.984-817A>C ENSP00000488924.1:n.984-817A>C
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