Canonical Allele Identifier: CA287485039
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs889769230
gnomAD v3: 17-7668172-C-T
gnomAD v4: 17-7668172-C-T
MyVariant Identifiers: chr17:g.7571490C>T (hg19) chr17:g.7668172C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668172C>T , CM000679.2:g.7668172C>T GRCh38
NC_000017.10:g.7571490C>T , CM000679.1:g.7571490C>T GRCh37
NC_000017.9:g.7512215C>T NCBI36
NG_017013.2:g.24379G>A , LRG_321:g.24379G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1928G>A ENSP00000352610.4:n.994-1928G>A
ENST00000413465.6:c.782+6009G>A ENSP00000410739.2:n.782+6009G>A
ENST00000635293.1:c.984-747G>A ENSP00000488924.1:n.984-747G>A
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