Canonical Allele Identifier: CA2635877195
Gene: TP53 HGNC NCBI

Linked Data

gnomAD v4: 17-7668334-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668334G>A , CM000679.2:g.7668334G>A GRCh38
NC_000017.10:g.7571652G>A , CM000679.1:g.7571652G>A GRCh37
NC_000017.9:g.7512377G>A NCBI36
NG_017013.2:g.24217C>T , LRG_321:g.24217C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2090C>T ENSP00000352610.4:n.994-2090C>T
ENST00000413465.6:c.782+5847C>T ENSP00000410739.2:n.782+5847C>T
ENST00000635293.1:c.984-909C>T ENSP00000488924.1:n.984-909C>T