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Canonical Allele Identifier:
CA16152484
Gene: PDCL3P4
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.101693134C>A
GRCh37
chr3:g.101411978C>A
Linked Data - Sequence & Population
gnomAD v2:
3:101411978 C / A
gnomAD v3:
3:101693134 C / A
gnomAD v4:
chr3-101693134-C-A
Joint Max Group AF
0.40429243 (AFR)
Genomes Max Group AF
0.40429243 (AFR)
Linked Data - NCBI & NCI
dbSNP:
112553552
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.101693134C>A , CM000665.2:g.101693134C>A
GRCh38
NC_000003.11:g.101411978C>A , CM000665.1:g.101411978C>A
GRCh37
NC_000003.10:g.102894668C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000667844.1:n.730+165C>A
ENST00000685383.1:n.697+165C>A
XM_011513341.1:c.253C>A
XP_011511643.1:p.Gln85Lys
XR_924279.1:n.192+5745C>A
XR_924280.1:n.70+165C>A
XR_924281.1:n.192+5745C>A
XM_011513341.3:c.253C>A
XP_011511643.1:p.Gln85Lys
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