Canonical Allele Identifier: CA775165349
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1468848836
gnomAD v3: 17-7668212-T-C
gnomAD v4: 17-7668212-T-C
MyVariant Identifiers: chr17:g.7571530T>C (hg19) chr17:g.7668212T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668212T>C , CM000679.2:g.7668212T>C GRCh38
NC_000017.10:g.7571530T>C , CM000679.1:g.7571530T>C GRCh37
NC_000017.9:g.7512255T>C NCBI36
NG_017013.2:g.24339A>G , LRG_321:g.24339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1968A>G ENSP00000352610.4:n.994-1968A>G
ENST00000413465.6:c.782+5969A>G ENSP00000410739.2:n.782+5969A>G
ENST00000635293.1:c.984-787A>G ENSP00000488924.1:n.984-787A>G
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