Canonical Allele Identifier: CA14394780
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1294447
ClinVar RCV Id: RCV001720351
dbSNP Id: rs1614984
gnomAD v2: 17-7571452-G-A
gnomAD v3: 17-7668134-G-A
gnomAD v4: 17-7668134-G-A
MyVariant Identifiers: chr17:g.7571452G>A (hg19) chr17:g.7668134G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668134G>A , CM000679.2:g.7668134G>A GRCh38
NC_000017.10:g.7571452G>A , CM000679.1:g.7571452G>A GRCh37
NC_000017.9:g.7512177G>A NCBI36
NG_017013.2:g.24417C>T , LRG_321:g.24417C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1890C>T ENSP00000352610.4:n.994-1890C>T
ENST00000413465.6:c.782+6047C>T ENSP00000410739.2:n.782+6047C>T
ENST00000635293.1:c.984-709C>T ENSP00000488924.1:n.984-709C>T
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