Canonical Allele Identifier: CA981206378
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs2072748297
gnomAD v3: 17-7668144-C-T
gnomAD v4: 17-7668144-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668144C>T , CM000679.2:g.7668144C>T GRCh38
NC_000017.10:g.7571462C>T , CM000679.1:g.7571462C>T GRCh37
NC_000017.9:g.7512187C>T NCBI36
NG_017013.2:g.24407G>A , LRG_321:g.24407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1900G>A ENSP00000352610.4:n.994-1900G>A
ENST00000413465.6:c.782+6037G>A ENSP00000410739.2:n.782+6037G>A
ENST00000635293.1:c.984-719G>A ENSP00000488924.1:n.984-719G>A
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