Canonical Allele Identifier: CA2892465

Gene: WDR19

Linked Data

• dbSNP Id: rs369571548
• ExAC: 4:39278623 A / G
• gnomAD v2: 4-39278623-A-G
• gnomAD v3: 4-39277003-A-G
• gnomAD v4: 4-39277003-A-G
• MyVariant Identifiers: chr4:g.39278623A>G (hg19) ; chr4:g.39277003A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277003A>G , CM000666.2:g.39277003A>G	GRCh38
NC_000004.11:g.39278623A>G , CM000666.1:g.39278623A>G	GRCh37
NC_000004.10:g.38955018A>G	NCBI36
NG_031813.1:g.99600A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3717-17A>G MANE Select	ENSP00000382717.3:n.3717-17A>G
ENST00000399820.7:c.3717-17A>G	ENSP00000382717.3:n.3717-17A>G
ENST00000503733.1:n.40A>G
ENST00000506869.5:c.*3298-17A>G	ENSP00000424319.1:n.*3298-17A>G
ENST00000512534.5:n.2028-17A>G
ENST00000512588.5:n.42A>G
NM_025132.3:c.3717-17A>G	NP_079408.3:n.3717-17A>G
XM_011513724.1:c.3729-17A>G	XP_011512026.1:n.3729-17A>G
XM_011513725.1:c.3663-17A>G	XP_011512027.1:n.3663-17A>G
XM_011513726.1:c.3249-17A>G	XP_011512028.1:n.3249-17A>G
XM_011513727.1:c.3249-17A>G	XP_011512029.1:n.3249-17A>G
XM_011513728.1:c.3237-17A>G	XP_011512030.1:n.3237-17A>G
XR_925155.1:n.5427-17A>G
NM_001317924.1:c.3237-17A>G	NP_001304853.1:n.3237-17A>G
XM_011513725.2:c.3663-17A>G	XP_011512027.1:n.3663-17A>G
XM_011513726.3:c.3249-17A>G	XP_011512028.1:n.3249-17A>G
XM_017008501.1:c.3237-17A>G	XP_016863990.1:n.3237-17A>G
XR_001741306.1:n.3994-17A>G
XR_001741307.1:n.3982-17A>G
XR_001741308.1:n.5628-17A>G
XR_001741309.1:n.5415-17A>G
XR_001741310.1:n.5616-17A>G
XR_001741311.2:n.5264-17A>G
NM_025132.4:c.3717-17A>G MANE Select	NP_079408.3:n.3717-17A>G
NM_001317924.2:c.3237-17A>G	NP_001304853.1:n.3237-17A>G