Canonical Allele Identifier: CA2672481785
Gene: PDGFC HGNC NCBI

Linked Data

gnomAD v4: 4-156762438-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.156762438G>T , CM000666.2:g.156762438G>T GRCh38
NC_000004.11:g.157683590G>T , CM000666.1:g.157683590G>T GRCh37
NC_000004.10:g.157903040G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000502773.6:c.*652C>A MANE Select ENSP00000422464.1:n.*652C>A
ENST00000274071.6:c.*1598C>A ENSP00000274071.2:n.*1598C>A
ENST00000502773.5:c.*652C>A ENSP00000422464.1:n.*652C>A
NM_016205.2:c.*652C>A NP_057289.1:n.*652C>A
NR_036641.1:n.2242C>A
XM_011532124.1:c.*652C>A XP_011530426.1:n.*652C>A
XM_011532125.1:c.*652C>A XP_011530427.1:n.*652C>A
XM_011532124.2:c.*652C>A XP_011530426.1:n.*652C>A
XM_017008455.1:c.*652C>A XP_016863944.1:n.*652C>A
XM_017008456.2:c.*652C>A XP_016863945.1:n.*652C>A
NM_016205.3:c.*652C>A MANE Select NP_057289.1:n.*652C>A
NR_036641.2:n.2647C>A
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