Canonical Allele Identifier: CA775165354
Gene: TP53 HGNC NCBI

Linked Data

dbSNP Id: rs1211245106
gnomAD v3: 17-7668223-A-C
gnomAD v4: 17-7668223-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668223A>C , CM000679.2:g.7668223A>C GRCh38
NC_000017.10:g.7571541A>C , CM000679.1:g.7571541A>C GRCh37
NC_000017.9:g.7512266A>C NCBI36
NG_017013.2:g.24328T>G , LRG_321:g.24328T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-1979T>G ENSP00000352610.4:n.994-1979T>G
ENST00000413465.6:c.782+5958T>G ENSP00000410739.2:n.782+5958T>G
ENST00000635293.1:c.984-798T>G ENSP00000488924.1:n.984-798T>G