Canonical Allele Identifier: CA2672481835

Gene: PDGFC

Linked Data

• gnomAD v4: 4-156762567-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762567T>G , CM000666.2:g.156762567T>G	GRCh38
NC_000004.11:g.157683719T>G , CM000666.1:g.157683719T>G	GRCh37
NC_000004.10:g.157903169T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.*523A>C MANE Select	ENSP00000422464.1:n.*523A>C
ENST00000274071.6:c.*1469A>C	ENSP00000274071.2:n.*1469A>C
ENST00000502773.5:c.*523A>C	ENSP00000422464.1:n.*523A>C
NM_016205.2:c.*523A>C	NP_057289.1:n.*523A>C
NR_036641.1:n.2113A>C
XM_011532124.1:c.*523A>C	XP_011530426.1:n.*523A>C
XM_011532125.1:c.*523A>C	XP_011530427.1:n.*523A>C
XM_011532124.2:c.*523A>C	XP_011530426.1:n.*523A>C
XM_017008455.1:c.*523A>C	XP_016863944.1:n.*523A>C
XM_017008456.2:c.*523A>C	XP_016863945.1:n.*523A>C
NM_016205.3:c.*523A>C MANE Select	NP_057289.1:n.*523A>C
NR_036641.2:n.2518A>C