Canonical Allele Identifier: CA2891724

Gene: WDR19

Linked Data

• ClinVar Variation Id: 446635
• ClinVar RCV Id: RCV000516052 ; RCV001851417
• dbSNP Id: rs377160857
• ExAC: 4:39207346 G / A
• gnomAD v2: 4-39207346-G-A
• gnomAD v3: 4-39205726-G-A
• gnomAD v4: 4-39205726-G-A
• MyVariant Identifiers: chr4:g.39207346G>A (hg19) ; chr4:g.39205726G>A (hg38)
• PubMed: PMID:29068549

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39205726G>A , CM000666.2:g.39205726G>A	GRCh38
NC_000004.11:g.39207346G>A , CM000666.1:g.39207346G>A	GRCh37
NC_000004.10:g.38883741G>A	NCBI36
NG_031813.1:g.28323G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.880G>A MANE Select	ENSP00000382717.3:p.Gly294Arg
ENST00000399820.7:c.880G>A	ENSP00000382717.3:p.Gly294Arg
ENST00000503697.5:c.*348G>A	ENSP00000423706.1:n.*348G>A
ENST00000506503.1:c.880G>A	ENSP00000423491.1:p.Gly294Arg
ENST00000506869.5:c.*461G>A	ENSP00000424319.1:n.*461G>A
ENST00000511729.5:n.41-22832G>A
ENST00000512448.1:n.474G>A
NM_025132.3:c.880G>A	NP_079408.3:p.Gly294Arg
XM_011513724.1:c.880G>A	XP_011512026.1:p.Gly294Arg
XM_011513725.1:c.814G>A	XP_011512027.1:p.Gly272Arg
XM_011513726.1:c.400G>A	XP_011512028.1:p.Gly134Arg
XM_011513727.1:c.400G>A	XP_011512029.1:p.Gly134Arg
XM_011513728.1:c.400G>A	XP_011512030.1:p.Gly134Arg
XM_011513729.1:c.880G>A	XP_011512031.1:p.Gly294Arg
XR_925155.1:n.944G>A
NM_001317924.1:c.400G>A	NP_001304853.1:p.Gly134Arg
XM_011513725.2:c.814G>A	XP_011512027.1:p.Gly272Arg
XM_011513726.3:c.400G>A	XP_011512028.1:p.Gly134Arg
XM_017008501.1:c.400G>A	XP_016863990.1:p.Gly134Arg
XR_001741306.1:n.944G>A
XR_001741307.1:n.944G>A
XR_001741308.1:n.944G>A
XR_001741309.1:n.944G>A
XR_001741310.1:n.944G>A
XR_001741311.2:n.793G>A
XR_001741312.1:n.944G>A
NM_025132.4:c.880G>A MANE Select	NP_079408.3:p.Gly294Arg
NM_001317924.2:c.400G>A	NP_001304853.1:p.Gly134Arg