Canonical Allele Identifier: CA2891831
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 261857
dbSNP Id: rs16995189
gnomAD v2: 4-39219593-T-C
gnomAD v3: 4-39217973-T-C
gnomAD v4: 4-39217973-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39217973T>C , CM000666.2:g.39217973T>C GRCh38
NC_000004.11:g.39219593T>C , CM000666.1:g.39219593T>C GRCh37
NC_000004.10:g.38895988T>C NCBI36
NG_031813.1:g.40570T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.1357-10T>C MANE Select ENSP00000382717.3:n.1357-10T>C
ENST00000399820.7:c.1357-10T>C ENSP00000382717.3:n.1357-10T>C
ENST00000506503.1:c.1357-14T>C ENSP00000423491.1:n.1357-14T>C
ENST00000506869.5:c.*938-10T>C ENSP00000424319.1:n.*938-10T>C
ENST00000511729.5:n.41-10585T>C
ENST00000512095.5:n.355-10T>C
NM_025132.3:c.1357-10T>C NP_079408.3:n.1357-10T>C
XM_011513724.1:c.1357-10T>C XP_011512026.1:n.1357-10T>C
XM_011513725.1:c.1291-10T>C XP_011512027.1:n.1291-10T>C
XM_011513726.1:c.877-10T>C XP_011512028.1:n.877-10T>C
XM_011513727.1:c.877-10T>C XP_011512029.1:n.877-10T>C
XM_011513728.1:c.877-10T>C XP_011512030.1:n.877-10T>C
XM_011513729.1:c.1357-10T>C XP_011512031.1:n.1357-10T>C
XR_925155.1:n.1421-10T>C
NM_001317924.1:c.877-10T>C NP_001304853.1:n.877-10T>C
XM_011513725.2:c.1291-10T>C XP_011512027.1:n.1291-10T>C
XM_011513726.3:c.877-10T>C XP_011512028.1:n.877-10T>C
XM_017008501.1:c.877-10T>C XP_016863990.1:n.877-10T>C
XR_001741306.1:n.1421-10T>C
XR_001741307.1:n.1421-10T>C
XR_001741308.1:n.1421-10T>C
XR_001741309.1:n.1421-10T>C
XR_001741310.1:n.1421-10T>C
XR_001741311.2:n.1270-10T>C
XR_001741312.1:n.1421-10T>C
NM_025132.4:c.1357-10T>C MANE Select NP_079408.3:n.1357-10T>C
NM_001317924.2:c.877-10T>C NP_001304853.1:n.877-10T>C