Canonical Allele Identifier: CA1931902843
Community Standard Title: NC_000010.11:g.100741814C=
Gene: PAX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.100741814C= , CM000672.2:g.100741814C= GRCh38
NC_000010.10:g.102501571C= , CM000672.1:g.102501571C= GRCh37
NC_000010.9:g.102491561C= NCBI36
NG_008680.1:g.1104C=
NG_008680.2:g.11106C=

Transcript Alleles

HGVS Amino-acid Change
NM_001304569.1:c.26-4379C= NP_001291498.1:n.26-4379C=
NM_001304569.2:c.26-4379C= NP_001291498.1:n.26-4379C=
NM_001374303.1:c.26-4379C= NP_001361232.1:n.26-4379C=
ENST00000553492.5:n.131+6081C=
ENST00000679374.1:c.25+6081C= ENSP00000506041.1:n.25+6081C=
ENST00000707078.1:c.26-4379C= ENSP00000516729.1:n.26-4379C=