Canonical Allele Identifier: CA1069887506

Gene: PDGFC

Linked Data

• dbSNP Id: rs1730404702
• gnomAD v3: 4-156762575-A-G
• gnomAD v4: 4-156762575-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.156762575A>G , CM000666.2:g.156762575A>G	GRCh38
NC_000004.11:g.157683727A>G , CM000666.1:g.157683727A>G	GRCh37
NC_000004.10:g.157903177A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000502773.6:c.*515T>C MANE Select	ENSP00000422464.1:n.*515T>C
ENST00000274071.6:c.*1461T>C	ENSP00000274071.2:n.*1461T>C
ENST00000502773.5:c.*515T>C	ENSP00000422464.1:n.*515T>C
NM_016205.2:c.*515T>C	NP_057289.1:n.*515T>C
NR_036641.1:n.2105T>C
XM_011532124.1:c.*515T>C	XP_011530426.1:n.*515T>C
XM_011532125.1:c.*515T>C	XP_011530427.1:n.*515T>C
XM_011532124.2:c.*515T>C	XP_011530426.1:n.*515T>C
XM_017008455.1:c.*515T>C	XP_016863944.1:n.*515T>C
XM_017008456.2:c.*515T>C	XP_016863945.1:n.*515T>C
NM_016205.3:c.*515T>C MANE Select	NP_057289.1:n.*515T>C
NR_036641.2:n.2510T>C