Canonical Allele Identifier: CA2635877139
Gene: TP53 HGNC NCBI

Linked Data

gnomAD v4: 17-7668315-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668315A>G , CM000679.2:g.7668315A>G GRCh38
NC_000017.10:g.7571633A>G , CM000679.1:g.7571633A>G GRCh37
NC_000017.9:g.7512358A>G NCBI36
NG_017013.2:g.24236T>C , LRG_321:g.24236T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2071T>C ENSP00000352610.4:n.994-2071T>C
ENST00000413465.6:c.782+5866T>C ENSP00000410739.2:n.782+5866T>C
ENST00000635293.1:c.984-890T>C ENSP00000488924.1:n.984-890T>C