Canonical Allele Identifier: CA438942070

Gene: WDR19

Linked Data

• dbSNP Id: rs1489023779
• gnomAD v2: 4-39246098-A-G
• gnomAD v4: 4-39244478-A-G
• MyVariant Identifiers: chr4:g.39246098A>G (hg19) ; chr4:g.39244478A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244478A>G , CM000666.2:g.39244478A>G	GRCh38
NC_000004.11:g.39246098A>G , CM000666.1:g.39246098A>G	GRCh37
NC_000004.10:g.38922493A>G	NCBI36
NG_031813.1:g.67075A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399820.8:c.2571A>G MANE Select	ENSP00000382717.3:p.Ser857=
ENST00000399820.7:c.2571A>G	ENSP00000382717.3:p.Ser857=
ENST00000506869.5:c.*2152A>G	ENSP00000424319.1:n.*2152A>G
ENST00000512095.5:n.1569A>G
NM_025132.3:c.2571A>G	NP_079408.3:p.Ser857=
XM_011513724.1:c.2583A>G	XP_011512026.1:p.Ser861=
XM_011513725.1:c.2517A>G	XP_011512027.1:p.Ser839=
XM_011513726.1:c.2103A>G	XP_011512028.1:p.Ser701=
XM_011513727.1:c.2103A>G	XP_011512029.1:p.Ser701=
XM_011513728.1:c.2091A>G	XP_011512030.1:p.Ser697=
XM_011513729.1:c.2583A>G	XP_011512031.1:p.Ser861=
XR_925155.1:n.2647A>G
NM_001317924.1:c.2091A>G	NP_001304853.1:p.Ser697=
XM_011513725.2:c.2517A>G	XP_011512027.1:p.Ser839=
XM_011513726.3:c.2103A>G	XP_011512028.1:p.Ser701=
XM_017008501.1:c.2091A>G	XP_016863990.1:p.Ser697=
XR_001741306.1:n.2647A>G
XR_001741307.1:n.2635A>G
XR_001741308.1:n.2647A>G
XR_001741309.1:n.2635A>G
XR_001741310.1:n.2635A>G
XR_001741311.2:n.2484A>G
NM_025132.4:c.2571A>G MANE Select	NP_079408.3:p.Ser857=
NM_001317924.2:c.2091A>G	NP_001304853.1:p.Ser697=