Canonical Allele Identifier: CA2892116
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446642
ClinVar RCV Id: RCV000515874
dbSNP Id: rs772599282

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.39244470C>T , CM000666.2:g.39244470C>T GRCh38
NC_000004.11:g.39246090C>T , CM000666.1:g.39246090C>T GRCh37
NC_000004.10:g.38922485C>T NCBI36
NG_031813.1:g.67067C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399820.8:c.2563C>T MANE Select ENSP00000382717.3:p.Gln855Ter
ENST00000399820.7:c.2563C>T ENSP00000382717.3:p.Gln855Ter
ENST00000506869.5:c.*2144C>T ENSP00000424319.1:p.=
ENST00000512095.5:n.1561C>T
NM_025132.3:c.2563C>T NP_079408.3:p.Gln855Ter
XM_011513724.1:c.2575C>T XP_011512026.1:p.Gln859Ter
XM_011513725.1:c.2509C>T XP_011512027.1:p.Gln837Ter
XM_011513726.1:c.2095C>T XP_011512028.1:p.Gln699Ter
XM_011513727.1:c.2095C>T XP_011512029.1:p.Gln699Ter
XM_011513728.1:c.2083C>T XP_011512030.1:p.Gln695Ter
XM_011513729.1:c.2575C>T XP_011512031.1:p.Gln859Ter
XR_925155.1:n.2639C>T
NM_001317924.1:c.2083C>T NP_001304853.1:p.Gln695Ter
XM_011513725.2:c.2509C>T XP_011512027.1:p.Gln837Ter
XM_011513726.3:c.2095C>T XP_011512028.1:p.Gln699Ter
XM_017008501.1:c.2083C>T XP_016863990.1:p.Gln695Ter
XR_001741306.1:n.2639C>T
XR_001741307.1:n.2627C>T
XR_001741308.1:n.2639C>T
XR_001741309.1:n.2627C>T
XR_001741310.1:n.2627C>T
XR_001741311.2:n.2476C>T
NM_025132.4:c.2563C>T MANE Select NP_079408.3:p.Gln855Ter
NM_001317924.2:c.2083C>T NP_001304853.1:p.Gln695Ter