Canonical Allele Identifier: CA2635877256
Gene: TP53 HGNC NCBI

Linked Data

gnomAD v4: 17-7668348-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668348G>A , CM000679.2:g.7668348G>A GRCh38
NC_000017.10:g.7571666G>A , CM000679.1:g.7571666G>A GRCh37
NC_000017.9:g.7512391G>A NCBI36
NG_017013.2:g.24203C>T , LRG_321:g.24203C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2104C>T ENSP00000352610.4:n.994-2104C>T
ENST00000413465.6:c.782+5833C>T ENSP00000410739.2:n.782+5833C>T
ENST00000635293.1:c.984-923C>T ENSP00000488924.1:n.984-923C>T