Canonical Allele Identifier: CA2635877167
Gene: TP53 HGNC NCBI

Linked Data

gnomAD v4: 17-7668320-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7668320C>A , CM000679.2:g.7668320C>A GRCh38
NC_000017.10:g.7571638C>A , CM000679.1:g.7571638C>A GRCh37
NC_000017.9:g.7512363C>A NCBI36
NG_017013.2:g.24231G>T , LRG_321:g.24231G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359597.8:c.994-2076G>T ENSP00000352610.4:n.994-2076G>T
ENST00000413465.6:c.782+5861G>T ENSP00000410739.2:n.782+5861G>T
ENST00000635293.1:c.984-895G>T ENSP00000488924.1:n.984-895G>T