Canonical Allele Identifier: CA2891690
Gene: WDR19 HGNC NCBI

Linked Data

dbSNP Id: rs527709762
gnomAD v2: 4-39207197-G-A
gnomAD v3: 4-39205577-G-A
gnomAD v4: 4-39205577-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205577G>A , CM000666.2:g.39205577G>A GRCh38
NC_000004.11:g.39207197G>A , CM000666.1:g.39207197G>A GRCh37
NC_000004.10:g.38883592G>A NCBI36
NG_031813.1:g.28174G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.731G>A MANE Select ENSP00000382717.3:p.Arg244His
ENST00000399820.7:c.731G>A ENSP00000382717.3:p.Arg244His
ENST00000503697.5:c.*199G>A ENSP00000423706.1:n.*199G>A
ENST00000506503.1:c.731G>A ENSP00000423491.1:p.Arg244His
ENST00000506869.5:c.*312G>A ENSP00000424319.1:n.*312G>A
ENST00000511729.5:n.41-22981G>A
ENST00000512448.1:n.325G>A
NM_025132.3:c.731G>A NP_079408.3:p.Arg244His
XM_011513724.1:c.731G>A XP_011512026.1:p.Arg244His
XM_011513725.1:c.665G>A XP_011512027.1:p.Arg222His
XM_011513726.1:c.251G>A XP_011512028.1:p.Arg84His
XM_011513727.1:c.251G>A XP_011512029.1:p.Arg84His
XM_011513728.1:c.251G>A XP_011512030.1:p.Arg84His
XM_011513729.1:c.731G>A XP_011512031.1:p.Arg244His
XR_925155.1:n.795G>A
NM_001317924.1:c.251G>A NP_001304853.1:p.Arg84His
XM_011513725.2:c.665G>A XP_011512027.1:p.Arg222His
XM_011513726.3:c.251G>A XP_011512028.1:p.Arg84His
XM_017008501.1:c.251G>A XP_016863990.1:p.Arg84His
XR_001741306.1:n.795G>A
XR_001741307.1:n.795G>A
XR_001741308.1:n.795G>A
XR_001741309.1:n.795G>A
XR_001741310.1:n.795G>A
XR_001741311.2:n.644G>A
XR_001741312.1:n.795G>A
NM_025132.4:c.731G>A MANE Select NP_079408.3:p.Arg244His
NM_001317924.2:c.251G>A NP_001304853.1:p.Arg84His