Canonical Allele Identifier: CA2724648835

Gene: PDGFD

Linked Data

• dbSNP Id: rs1858505168

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103937341A>C , CM000673.2:g.103937341A>C	GRCh38
NC_000011.9:g.103808069A>C , CM000673.1:g.103808069A>C	GRCh37
NC_000011.8:g.103313279A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393158.7:c.772+6111T>G MANE Select	ENSP00000376865.2:n.772+6111T>G
ENST00000302251.9:c.754+6111T>G	ENSP00000302193.5:n.754+6111T>G
ENST00000393158.6:c.772+6111T>G	ENSP00000376865.2:n.772+6111T>G
NM_025208.4:c.772+6111T>G	NP_079484.1:n.772+6111T>G
NM_033135.3:c.754+6111T>G	NP_149126.1:n.754+6111T>G
NM_025208.5:c.772+6111T>G MANE Select	NP_079484.1:n.772+6111T>G
NM_033135.4:c.754+6111T>G	NP_149126.1:n.754+6111T>G