Canonical Allele Identifier: CA1505986215

Gene: PDGFC

Linked Data

• dbSNP Id: rs1051340807

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156798985C>G , CM000666.2:g.156798985C>G	GRCh38
NC_000004.11:g.157720137C>G , CM000666.1:g.157720137C>G	GRCh37
NC_000004.10:g.157939587C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502773.6:c.495+11852G>C MANE Select	ENSP00000422464.1:n.495+11852G>C
ENST00000274071.6:c.*403+11852G>C	ENSP00000274071.2:n.*403+11852G>C
ENST00000422544.2:c.495+11852G>C	ENSP00000410048.2:n.495+11852G>C
ENST00000502773.5:c.495+11852G>C	ENSP00000422464.1:n.495+11852G>C
ENST00000506880.5:c.149+11852G>C
ENST00000511985.1:n.55+11852G>C
ENST00000512711.1:n.418-26092G>C
NM_016205.2:c.495+11852G>C	NP_057289.1:n.495+11852G>C
NR_036641.1:n.1047+11852G>C
XM_011532124.1:c.462+11852G>C	XP_011530426.1:n.462+11852G>C
XM_011532125.1:c.426+11852G>C	XP_011530427.1:n.426+11852G>C
XM_011532124.2:c.462+11852G>C	XP_011530426.1:n.462+11852G>C
XM_017008455.1:c.390+11852G>C	XP_016863944.1:n.390+11852G>C
XM_017008456.2:c.495+11852G>C	XP_016863945.1:n.495+11852G>C
NM_016205.3:c.495+11852G>C MANE Select	NP_057289.1:n.495+11852G>C
NR_036641.2:n.1452+11852G>C