Canonical Allele Identifier: CA14459941
Gene: TP53 HGNC NCBI
COSMIC:
COSN6661030 (not active)
MyVariant.info:
GRCh38 chr17:g.7667753T>C
GRCh37 chr17:g.7571071T>C
gnomAD v2:
17:7571071 T / C
gnomAD v3:
17:7667753 T / C
gnomAD v4:
chr17-7667753-T-C
Joint Max Group AF 0.34271881 (EAS)
Genomes Max Group AF 0.34271881 (EAS)
dbSNP:
17887200
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7667753T>C , CM000679.2:g.7667753T>C GRCh38
NC_000017.10:g.7571071T>C , CM000679.1:g.7571071T>C GRCh37
NC_000017.9:g.7511796T>C NCBI36
NG_017013.2:g.24798A>G , LRG_321:g.24798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359597.8:c.994-1509A>G ENSP00000352610.4:n.994-1509A>G
ENST00000413465.6:c.783-5739A>G ENSP00000410739.2:n.783-5739A>G
ENST00000635293.1:c.984-328A>G ENSP00000488924.1:n.984-328A>G
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