Canonical Allele Identifier: CA775165319
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1177563849
MyVariant Identifiers: chr17:g.7571482G>C (hg19) chr17:g.7668164G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668164G>C , CM000679.2:g.7668164G>C GRCh38
NC_000017.10:g.7571482G>C , CM000679.1:g.7571482G>C GRCh37
NC_000017.9:g.7512207G>C NCBI36
NG_017013.2:g.24387C>G , LRG_321:g.24387C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1920C>G ENSP00000352610.4:n.994-1920C>G
ENST00000413465.6:c.782+6017C>G ENSP00000410739.2:n.782+6017C>G
ENST00000635293.1:c.984-739C>G ENSP00000488924.1:n.984-739C>G
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