Canonical Allele Identifier: CA2892487

Gene: WDR19

Linked Data

• dbSNP Id: rs756519107
• ExAC: 4:39278726 C / G
• gnomAD v2: 4-39278726-C-G
• gnomAD v4: 4-39277106-C-G
• MyVariant Identifiers: chr4:g.39278726C>G (hg19) ; chr4:g.39277106C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277106C>G , CM000666.2:g.39277106C>G	GRCh38
NC_000004.11:g.39278726C>G , CM000666.1:g.39278726C>G	GRCh37
NC_000004.10:g.38955121C>G	NCBI36
NG_031813.1:g.99703C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.3803C>G MANE Select	ENSP00000382717.3:p.Pro1268Arg
ENST00000399820.7:c.3803C>G	ENSP00000382717.3:p.Pro1268Arg
ENST00000503733.1:n.143C>G
ENST00000506869.5:c.*3384C>G	ENSP00000424319.1:n.*3384C>G
ENST00000512534.5:n.2114C>G
ENST00000512588.5:n.145C>G
NM_025132.3:c.3803C>G	NP_079408.3:p.Pro1268Arg
XM_011513724.1:c.3815C>G	XP_011512026.1:p.Pro1272Arg
XM_011513725.1:c.3749C>G	XP_011512027.1:p.Pro1250Arg
XM_011513726.1:c.3335C>G	XP_011512028.1:p.Pro1112Arg
XM_011513727.1:c.3335C>G	XP_011512029.1:p.Pro1112Arg
XM_011513728.1:c.3323C>G	XP_011512030.1:p.Pro1108Arg
XR_925155.1:n.5513C>G
NM_001317924.1:c.3323C>G	NP_001304853.1:p.Pro1108Arg
XM_011513725.2:c.3749C>G	XP_011512027.1:p.Pro1250Arg
XM_011513726.3:c.3335C>G	XP_011512028.1:p.Pro1112Arg
XM_017008501.1:c.3323C>G	XP_016863990.1:p.Pro1108Arg
XR_001741306.1:n.4080C>G
XR_001741307.1:n.4068C>G
XR_001741308.1:n.5714C>G
XR_001741309.1:n.5501C>G
XR_001741310.1:n.5702C>G
XR_001741311.2:n.5350C>G
NM_025132.4:c.3803C>G MANE Select	NP_079408.3:p.Pro1268Arg
NM_001317924.2:c.3323C>G	NP_001304853.1:p.Pro1108Arg