Canonical Allele Identifier: CA2891714
Gene: WDR19 HGNC NCBI

Linked Data

dbSNP Id: rs760748596
gnomAD v2: 4-39207293-A-G
gnomAD v4: 4-39205673-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39205673A>G , CM000666.2:g.39205673A>G GRCh38
NC_000004.11:g.39207293A>G , CM000666.1:g.39207293A>G GRCh37
NC_000004.10:g.38883688A>G NCBI36
NG_031813.1:g.28270A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399820.8:c.827A>G MANE Select ENSP00000382717.3:p.Asp276Gly
ENST00000399820.7:c.827A>G ENSP00000382717.3:p.Asp276Gly
ENST00000503697.5:c.*295A>G ENSP00000423706.1:n.*295A>G
ENST00000506503.1:c.827A>G ENSP00000423491.1:p.Asp276Gly
ENST00000506869.5:c.*408A>G ENSP00000424319.1:n.*408A>G
ENST00000511729.5:n.41-22885A>G
ENST00000512448.1:n.421A>G
NM_025132.3:c.827A>G NP_079408.3:p.Asp276Gly
XM_011513724.1:c.827A>G XP_011512026.1:p.Asp276Gly
XM_011513725.1:c.761A>G XP_011512027.1:p.Asp254Gly
XM_011513726.1:c.347A>G XP_011512028.1:p.Asp116Gly
XM_011513727.1:c.347A>G XP_011512029.1:p.Asp116Gly
XM_011513728.1:c.347A>G XP_011512030.1:p.Asp116Gly
XM_011513729.1:c.827A>G XP_011512031.1:p.Asp276Gly
XR_925155.1:n.891A>G
NM_001317924.1:c.347A>G NP_001304853.1:p.Asp116Gly
XM_011513725.2:c.761A>G XP_011512027.1:p.Asp254Gly
XM_011513726.3:c.347A>G XP_011512028.1:p.Asp116Gly
XM_017008501.1:c.347A>G XP_016863990.1:p.Asp116Gly
XR_001741306.1:n.891A>G
XR_001741307.1:n.891A>G
XR_001741308.1:n.891A>G
XR_001741309.1:n.891A>G
XR_001741310.1:n.891A>G
XR_001741311.2:n.740A>G
XR_001741312.1:n.891A>G
NM_025132.4:c.827A>G MANE Select NP_079408.3:p.Asp276Gly
NM_001317924.2:c.347A>G NP_001304853.1:p.Asp116Gly