Canonical Allele Identifier: CA1014600110
Gene: PGBD2 HGNC NCBI

Linked Data

dbSNP Id: rs1660997519

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.248874150A>C , CM000663.2:g.248874150A>C GRCh38
NC_000001.10:g.249168349A>C , CM000663.1:g.249168349A>C GRCh37
NC_000001.9:g.247134972A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011544160.1:c.-102+258A>C XP_011542462.1:n.-102+258A>C
XM_011544161.1:c.-48+258A>C XP_011542463.1:n.-48+258A>C
XM_011544161.3:c.-48+258A>C XP_011542463.1:n.-48+258A>C