Canonical Allele Identifier: CA1232724255
Gene: PGBD2 HGNC NCBI

Linked Data

dbSNP Id: rs1660997086

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.248874141A>G , CM000663.2:g.248874141A>G GRCh38
NC_000001.10:g.249168340A>G , CM000663.1:g.249168340A>G GRCh37
NC_000001.9:g.247134963A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011544160.1:c.-102+249A>G XP_011542462.1:n.-102+249A>G
XM_011544161.1:c.-48+249A>G XP_011542463.1:n.-48+249A>G
XM_011544161.3:c.-48+249A>G XP_011542463.1:n.-48+249A>G