Canonical Allele Identifier: CA775165353

Gene: TP53

Linked Data

• dbSNP Id: rs1211245106
• gnomAD v3: 17-7668223-A-G
• gnomAD v4: 17-7668223-A-G
• MyVariant Identifiers: chr17:g.7571541A>G (hg19) ; chr17:g.7668223A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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