Canonical Allele Identifier: CA287485016
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1037209585
gnomAD v2: 17-7571411-C-T
gnomAD v3: 17-7668093-C-T
gnomAD v4: 17-7668093-C-T
MyVariant Identifiers: chr17:g.7571411C>T (hg19) chr17:g.7668093C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668093C>T , CM000679.2:g.7668093C>T GRCh38
NC_000017.10:g.7571411C>T , CM000679.1:g.7571411C>T GRCh37
NC_000017.9:g.7512136C>T NCBI36
NG_017013.2:g.24458G>A , LRG_321:g.24458G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1849G>A ENSP00000352610.4:n.994-1849G>A
ENST00000413465.6:c.783-6079G>A ENSP00000410739.2:n.783-6079G>A
ENST00000635293.1:c.984-668G>A ENSP00000488924.1:n.984-668G>A
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