Canonical Allele Identifier: CA775165320

Gene: TP53

Linked Data

• dbSNP Id: rs1364965152
• gnomAD v3: 17-7668166-G-A
• gnomAD v4: 17-7668166-G-A
• MyVariant Identifiers: chr17:g.7571484G>A (hg19) ; chr17:g.7668166G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7668166G>A , CM000679.2:g.7668166G>A	GRCh38
NC_000017.10:g.7571484G>A , CM000679.1:g.7571484G>A	GRCh37
NC_000017.9:g.7512209G>A	NCBI36
NG_017013.2:g.24385C>T , LRG_321:g.24385C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359597.8:c.994-1922C>T	ENSP00000352610.4:n.994-1922C>T
ENST00000413465.6:c.782+6015C>T	ENSP00000410739.2:n.782+6015C>T
ENST00000635293.1:c.984-741C>T	ENSP00000488924.1:n.984-741C>T