Canonical Allele Identifier: CA1996762688

Gene: PDGFD

Linked Data

• dbSNP Id: rs1858503836

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103937242C>A , CM000673.2:g.103937242C>A	GRCh38
NC_000011.9:g.103807970C>A , CM000673.1:g.103807970C>A	GRCh37
NC_000011.8:g.103313180C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393158.7:c.772+6210G>T MANE Select	ENSP00000376865.2:n.772+6210G>T
ENST00000302251.9:c.754+6210G>T	ENSP00000302193.5:n.754+6210G>T
ENST00000393158.6:c.772+6210G>T	ENSP00000376865.2:n.772+6210G>T
NM_025208.4:c.772+6210G>T	NP_079484.1:n.772+6210G>T
NM_033135.3:c.754+6210G>T	NP_149126.1:n.754+6210G>T
NM_025208.5:c.772+6210G>T MANE Select	NP_079484.1:n.772+6210G>T
NM_033135.4:c.754+6210G>T	NP_149126.1:n.754+6210G>T