Canonical Allele Identifier: CA95686083

Gene: WDR19

Linked Data

• ClinVar Variation Id: 1924598
• ClinVar RCV Id: RCV002634870
• dbSNP Id: rs913477341
• MyVariant Identifiers: chr4:g.39206798A>G (hg19) ; chr4:g.39205178A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205178A>G , CM000666.2:g.39205178A>G	GRCh38
NC_000004.11:g.39206798A>G , CM000666.1:g.39206798A>G	GRCh37
NC_000004.10:g.38883193A>G	NCBI36
NG_031813.1:g.27775A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.628A>G MANE Select	ENSP00000382717.3:p.Thr210Ala
ENST00000399820.7:c.628A>G	ENSP00000382717.3:p.Thr210Ala
ENST00000503697.5:c.*96A>G	ENSP00000423706.1:n.*96A>G
ENST00000505055.5:c.*209A>G	ENSP00000425949.1:n.*209A>G
ENST00000506503.1:c.628A>G	ENSP00000423491.1:p.Thr210Ala
ENST00000506869.5:c.*209A>G	ENSP00000424319.1:n.*209A>G
ENST00000511729.5:n.40+22615A>G
ENST00000512448.1:n.222A>G
NM_025132.3:c.628A>G	NP_079408.3:p.Thr210Ala
XM_011513724.1:c.628A>G	XP_011512026.1:p.Thr210Ala
XM_011513725.1:c.562A>G	XP_011512027.1:p.Thr188Ala
XM_011513726.1:c.148A>G	XP_011512028.1:p.Thr50Ala
XM_011513727.1:c.148A>G	XP_011512029.1:p.Thr50Ala
XM_011513728.1:c.148A>G	XP_011512030.1:p.Thr50Ala
XM_011513729.1:c.628A>G	XP_011512031.1:p.Thr210Ala
XR_925155.1:n.692A>G
NM_001317924.1:c.148A>G	NP_001304853.1:p.Thr50Ala
XM_011513725.2:c.562A>G	XP_011512027.1:p.Thr188Ala
XM_011513726.3:c.148A>G	XP_011512028.1:p.Thr50Ala
XM_017008501.1:c.148A>G	XP_016863990.1:p.Thr50Ala
XR_001741306.1:n.692A>G
XR_001741307.1:n.692A>G
XR_001741308.1:n.692A>G
XR_001741309.1:n.692A>G
XR_001741310.1:n.692A>G
XR_001741311.2:n.541A>G
XR_001741312.1:n.692A>G
NM_025132.4:c.628A>G MANE Select	NP_079408.3:p.Thr210Ala
NM_001317924.2:c.148A>G	NP_001304853.1:p.Thr50Ala