Canonical Allele Identifier: CA1428414172
Gene: TP63 HGNC NCBI

Linked Data

dbSNP Id: rs7610017

Genomic Alleles

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

Transcript Alleles

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