Canonical Allele Identifier: CA789566914

Gene: PDGFC

Linked Data

• dbSNP Id: rs1267933749
• MyVariant Identifiers: chr4:g.157683701C>G (hg19) ; chr4:g.156762549C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762549C>G , CM000666.2:g.156762549C>G	GRCh38
NC_000004.11:g.157683701C>G , CM000666.1:g.157683701C>G	GRCh37
NC_000004.10:g.157903151C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.*541G>C MANE Select	ENSP00000422464.1:n.*541G>C
ENST00000274071.6:c.*1487G>C	ENSP00000274071.2:n.*1487G>C
ENST00000502773.5:c.*541G>C	ENSP00000422464.1:n.*541G>C
NM_016205.2:c.*541G>C	NP_057289.1:n.*541G>C
NR_036641.1:n.2131G>C
XM_011532124.1:c.*541G>C	XP_011530426.1:n.*541G>C
XM_011532125.1:c.*541G>C	XP_011530427.1:n.*541G>C
XM_011532124.2:c.*541G>C	XP_011530426.1:n.*541G>C
XM_017008455.1:c.*541G>C	XP_016863944.1:n.*541G>C
XM_017008456.2:c.*541G>C	XP_016863945.1:n.*541G>C
NM_016205.3:c.*541G>C MANE Select	NP_057289.1:n.*541G>C
NR_036641.2:n.2536G>C