Canonical Allele Identifier: CA2892080

Gene: WDR19

Linked Data

• ClinVar Variation Id: 1095954
• ClinVar RCV Id: RCV001417022
• dbSNP Id: rs564271912
• ExAC: 4:39245853 G / A
• gnomAD v2: 4-39245853-G-A
• gnomAD v3: 4-39244233-G-A
• gnomAD v4: 4-39244233-G-A
• MyVariant Identifiers: chr4:g.39245853G>A (hg19) ; chr4:g.39244233G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244233G>A , CM000666.2:g.39244233G>A	GRCh38
NC_000004.11:g.39245853G>A , CM000666.1:g.39245853G>A	GRCh37
NC_000004.10:g.38922248G>A	NCBI36
NG_031813.1:g.66830G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2422-15G>A MANE Select	ENSP00000382717.3:n.2422-15G>A
ENST00000399820.7:c.2422-15G>A	ENSP00000382717.3:n.2422-15G>A
ENST00000506869.5:c.*2003-15G>A	ENSP00000424319.1:n.*2003-15G>A
ENST00000512095.5:n.1420-15G>A
NM_025132.3:c.2422-15G>A	NP_079408.3:n.2422-15G>A
XM_011513724.1:c.2434-15G>A	XP_011512026.1:n.2434-15G>A
XM_011513725.1:c.2368-15G>A	XP_011512027.1:n.2368-15G>A
XM_011513726.1:c.1954-15G>A	XP_011512028.1:n.1954-15G>A
XM_011513727.1:c.1954-15G>A	XP_011512029.1:n.1954-15G>A
XM_011513728.1:c.1942-15G>A	XP_011512030.1:n.1942-15G>A
XM_011513729.1:c.2434-15G>A	XP_011512031.1:n.2434-15G>A
XR_925155.1:n.2498-15G>A
NM_001317924.1:c.1942-15G>A	NP_001304853.1:n.1942-15G>A
XM_011513725.2:c.2368-15G>A	XP_011512027.1:n.2368-15G>A
XM_011513726.3:c.1954-15G>A	XP_011512028.1:n.1954-15G>A
XM_017008501.1:c.1942-15G>A	XP_016863990.1:n.1942-15G>A
XR_001741306.1:n.2498-15G>A
XR_001741307.1:n.2486-15G>A
XR_001741308.1:n.2498-15G>A
XR_001741309.1:n.2486-15G>A
XR_001741310.1:n.2486-15G>A
XR_001741311.2:n.2335-15G>A
NM_025132.4:c.2422-15G>A MANE Select	NP_079408.3:n.2422-15G>A
NM_001317924.2:c.1942-15G>A	NP_001304853.1:n.1942-15G>A