Canonical Allele Identifier: CA356651549

Gene: WDR19

Linked Data

• dbSNP Id: rs1209319543
• gnomAD v2: 4-39278644-C-T
• MyVariant Identifiers: chr4:g.39278644C>T (hg19) ; chr4:g.39277024C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39277024C>T , CM000666.2:g.39277024C>T	GRCh38
NC_000004.11:g.39278644C>T , CM000666.1:g.39278644C>T	GRCh37
NC_000004.10:g.38955039C>T	NCBI36
NG_031813.1:g.99621C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.3721C>T MANE Select	ENSP00000382717.3:p.Pro1241Ser
ENST00000399820.7:c.3721C>T	ENSP00000382717.3:p.Pro1241Ser
ENST00000503733.1:n.61C>T
ENST00000506869.5:c.*3302C>T	ENSP00000424319.1:n.*3302C>T
ENST00000512534.5:n.2032C>T
ENST00000512588.5:n.63C>T
NM_025132.3:c.3721C>T	NP_079408.3:p.Pro1241Ser
XM_011513724.1:c.3733C>T	XP_011512026.1:p.Pro1245Ser
XM_011513725.1:c.3667C>T	XP_011512027.1:p.Pro1223Ser
XM_011513726.1:c.3253C>T	XP_011512028.1:p.Pro1085Ser
XM_011513727.1:c.3253C>T	XP_011512029.1:p.Pro1085Ser
XM_011513728.1:c.3241C>T	XP_011512030.1:p.Pro1081Ser
XR_925155.1:n.5431C>T
NM_001317924.1:c.3241C>T	NP_001304853.1:p.Pro1081Ser
XM_011513725.2:c.3667C>T	XP_011512027.1:p.Pro1223Ser
XM_011513726.3:c.3253C>T	XP_011512028.1:p.Pro1085Ser
XM_017008501.1:c.3241C>T	XP_016863990.1:p.Pro1081Ser
XR_001741306.1:n.3998C>T
XR_001741307.1:n.3986C>T
XR_001741308.1:n.5632C>T
XR_001741309.1:n.5419C>T
XR_001741310.1:n.5620C>T
XR_001741311.2:n.5268C>T
NM_025132.4:c.3721C>T MANE Select	NP_079408.3:p.Pro1241Ser
NM_001317924.2:c.3241C>T	NP_001304853.1:p.Pro1081Ser