Canonical Allele Identifier: CA1232724260
Gene: PGBD2 HGNC NCBI

Linked Data

dbSNP Id: rs1660997371

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.248874146C>T , CM000663.2:g.248874146C>T GRCh38
NC_000001.10:g.249168345C>T , CM000663.1:g.249168345C>T GRCh37
NC_000001.9:g.247134968C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011544160.1:c.-102+254C>T XP_011542462.1:n.-102+254C>T
XM_011544161.1:c.-48+254C>T XP_011542463.1:n.-48+254C>T
XM_011544161.3:c.-48+254C>T XP_011542463.1:n.-48+254C>T