Canonical Allele Identifier: CA1996762775

Gene: PDGFD

Linked Data

• dbSNP Id: rs10895547

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.103937424C>G , CM000673.2:g.103937424C>G	GRCh38
NC_000011.9:g.103808152C>G , CM000673.1:g.103808152C>G	GRCh37
NC_000011.8:g.103313362C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393158.7:c.772+6028G>C MANE Select	ENSP00000376865.2:n.772+6028G>C
ENST00000302251.9:c.754+6028G>C	ENSP00000302193.5:n.754+6028G>C
ENST00000393158.6:c.772+6028G>C	ENSP00000376865.2:n.772+6028G>C
NM_025208.4:c.772+6028G>C	NP_079484.1:n.772+6028G>C
NM_033135.3:c.754+6028G>C	NP_149126.1:n.754+6028G>C
NM_025208.5:c.772+6028G>C MANE Select	NP_079484.1:n.772+6028G>C
NM_033135.4:c.754+6028G>C	NP_149126.1:n.754+6028G>C