Canonical Allele Identifier: CA1232724267
Gene: PGBD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.248874155T= , CM000663.2:g.248874155T= GRCh38
NC_000001.10:g.249168354T= , CM000663.1:g.249168354T= GRCh37
NC_000001.9:g.247134977T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011544160.1:c.-102+263T= XP_011542462.1:n.-102+263T=
XM_011544161.1:c.-48+263T= XP_011542463.1:n.-48+263T=
XM_011544161.3:c.-48+263T= XP_011542463.1:n.-48+263T=