Canonical Allele Identifier: CA550722738

Gene: WDR19

Linked Data

• ClinVar Variation Id: 2924138
• ClinVar RCV Id: RCV003785888
• dbSNP Id: rs1243716998
• gnomAD v2: 4-39278625-G-A
• gnomAD v3: 4-39277005-G-A
• gnomAD v4: 4-39277005-G-A
• MyVariant Identifiers: chr4:g.39278625G>A (hg19) ; chr4:g.39277005G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277005G>A , CM000666.2:g.39277005G>A	GRCh38
NC_000004.11:g.39278625G>A , CM000666.1:g.39278625G>A	GRCh37
NC_000004.10:g.38955020G>A	NCBI36
NG_031813.1:g.99602G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3717-15G>A MANE Select	ENSP00000382717.3:n.3717-15G>A
ENST00000399820.7:c.3717-15G>A	ENSP00000382717.3:n.3717-15G>A
ENST00000503733.1:n.42G>A
ENST00000506869.5:c.*3298-15G>A	ENSP00000424319.1:n.*3298-15G>A
ENST00000512534.5:n.2028-15G>A
ENST00000512588.5:n.44G>A
NM_025132.3:c.3717-15G>A	NP_079408.3:n.3717-15G>A
XM_011513724.1:c.3729-15G>A	XP_011512026.1:n.3729-15G>A
XM_011513725.1:c.3663-15G>A	XP_011512027.1:n.3663-15G>A
XM_011513726.1:c.3249-15G>A	XP_011512028.1:n.3249-15G>A
XM_011513727.1:c.3249-15G>A	XP_011512029.1:n.3249-15G>A
XM_011513728.1:c.3237-15G>A	XP_011512030.1:n.3237-15G>A
XR_925155.1:n.5427-15G>A
NM_001317924.1:c.3237-15G>A	NP_001304853.1:n.3237-15G>A
XM_011513725.2:c.3663-15G>A	XP_011512027.1:n.3663-15G>A
XM_011513726.3:c.3249-15G>A	XP_011512028.1:n.3249-15G>A
XM_017008501.1:c.3237-15G>A	XP_016863990.1:n.3237-15G>A
XR_001741306.1:n.3994-15G>A
XR_001741307.1:n.3982-15G>A
XR_001741308.1:n.5628-15G>A
XR_001741309.1:n.5415-15G>A
XR_001741310.1:n.5616-15G>A
XR_001741311.2:n.5264-15G>A
NM_025132.4:c.3717-15G>A MANE Select	NP_079408.3:n.3717-15G>A
NM_001317924.2:c.3237-15G>A	NP_001304853.1:n.3237-15G>A