Canonical Allele Identifier: CA904187797

Gene: TP63

Linked Data

• dbSNP Id: rs7610017
• MyVariant Identifiers: chr3:g.189343424A>T (hg19) ; chr3:g.189625635A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189625635A>T , CM000665.2:g.189625635A>T	GRCh38
NC_000003.11:g.189343424A>T , CM000665.1:g.189343424A>T	GRCh37
NC_000003.10:g.190826118A>T	NCBI36
NG_007550.3:g.33890A>T

Transcript Alleles

HGVS	Amino-acid change
XM_011513251.1:c.59+2318A>T	XP_011511553.1:n.59+2318A>T
XM_011513252.1:c.56+28397A>T	XP_011511554.1:n.56+28397A>T
XM_011513253.1:c.23+58740A>T	XP_011511555.1:n.23+58740A>T
NM_001329964.1:c.56+28397A>T	NP_001316893.1:n.56+28397A>T
NM_001329964.2:c.56+28397A>T	NP_001316893.1:n.56+28397A>T