Canonical Allele Identifier: CA1666069956
Gene: PDE7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.135812521T= , CM000668.2:g.135812521T= GRCh38
NC_000006.11:g.136133659T= , CM000668.1:g.136133659T= GRCh37
NC_000006.10:g.136175352T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011535755.1:c.138+2545T= XP_011534057.1:n.138+2545T=