Canonical Allele Identifier: CA16618045
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 424471
ClinVar RCV Id: RCV000484356
dbSNP Id: rs1064796985
MyVariant Identifiers: chr4:g.39207208G>A (hg19) chr4:g.39205588G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205588G>A , CM000666.2:g.39205588G>A GRCh38
NC_000004.11:g.39207208G>A , CM000666.1:g.39207208G>A GRCh37
NC_000004.10:g.38883603G>A NCBI36
NG_031813.1:g.28185G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.742G>A MANE Select ENSP00000382717.3:p.Gly248Ser
ENST00000399820.7:c.742G>A ENSP00000382717.3:p.Gly248Ser
ENST00000503697.5:c.*210G>A ENSP00000423706.1:n.*210G>A
ENST00000506503.1:c.742G>A ENSP00000423491.1:p.Gly248Ser
ENST00000506869.5:c.*323G>A ENSP00000424319.1:n.*323G>A
ENST00000511729.5:n.41-22970G>A
ENST00000512448.1:n.336G>A
NM_025132.3:c.742G>A NP_079408.3:p.Gly248Ser
XM_011513724.1:c.742G>A XP_011512026.1:p.Gly248Ser
XM_011513725.1:c.676G>A XP_011512027.1:p.Gly226Ser
XM_011513726.1:c.262G>A XP_011512028.1:p.Gly88Ser
XM_011513727.1:c.262G>A XP_011512029.1:p.Gly88Ser
XM_011513728.1:c.262G>A XP_011512030.1:p.Gly88Ser
XM_011513729.1:c.742G>A XP_011512031.1:p.Gly248Ser
XR_925155.1:n.806G>A
NM_001317924.1:c.262G>A NP_001304853.1:p.Gly88Ser
XM_011513725.2:c.676G>A XP_011512027.1:p.Gly226Ser
XM_011513726.3:c.262G>A XP_011512028.1:p.Gly88Ser
XM_017008501.1:c.262G>A XP_016863990.1:p.Gly88Ser
XR_001741306.1:n.806G>A
XR_001741307.1:n.806G>A
XR_001741308.1:n.806G>A
XR_001741309.1:n.806G>A
XR_001741310.1:n.806G>A
XR_001741311.2:n.655G>A
XR_001741312.1:n.806G>A
NM_025132.4:c.742G>A MANE Select NP_079408.3:p.Gly248Ser
NM_001317924.2:c.262G>A NP_001304853.1:p.Gly88Ser
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