Canonical Allele Identifier: CA794682649

Gene: WDR19

Linked Data

• dbSNP Id: rs1337218454
• gnomAD v4: 4-39244165-T-C
• MyVariant Identifiers: chr4:g.39245785T>C (hg19) ; chr4:g.39244165T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.39244165T>C , CM000666.2:g.39244165T>C	GRCh38
NC_000004.11:g.39245785T>C , CM000666.1:g.39245785T>C	GRCh37
NC_000004.10:g.38922180T>C	NCBI36
NG_031813.1:g.66762T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399820.8:c.2422-83T>C MANE Select	ENSP00000382717.3:n.2422-83T>C
ENST00000399820.7:c.2422-83T>C	ENSP00000382717.3:n.2422-83T>C
ENST00000506869.5:c.*2003-83T>C	ENSP00000424319.1:n.*2003-83T>C
ENST00000512095.5:n.1420-83T>C
NM_025132.3:c.2422-83T>C	NP_079408.3:n.2422-83T>C
XM_011513724.1:c.2434-83T>C	XP_011512026.1:n.2434-83T>C
XM_011513725.1:c.2368-83T>C	XP_011512027.1:n.2368-83T>C
XM_011513726.1:c.1954-83T>C	XP_011512028.1:n.1954-83T>C
XM_011513727.1:c.1954-83T>C	XP_011512029.1:n.1954-83T>C
XM_011513728.1:c.1942-83T>C	XP_011512030.1:n.1942-83T>C
XM_011513729.1:c.2434-83T>C	XP_011512031.1:n.2434-83T>C
XR_925155.1:n.2498-83T>C
NM_001317924.1:c.1942-83T>C	NP_001304853.1:n.1942-83T>C
XM_011513725.2:c.2368-83T>C	XP_011512027.1:n.2368-83T>C
XM_011513726.3:c.1954-83T>C	XP_011512028.1:n.1954-83T>C
XM_017008501.1:c.1942-83T>C	XP_016863990.1:n.1942-83T>C
XR_001741306.1:n.2498-83T>C
XR_001741307.1:n.2486-83T>C
XR_001741308.1:n.2498-83T>C
XR_001741309.1:n.2486-83T>C
XR_001741310.1:n.2486-83T>C
XR_001741311.2:n.2335-83T>C
NM_025132.4:c.2422-83T>C MANE Select	NP_079408.3:n.2422-83T>C
NM_001317924.2:c.1942-83T>C	NP_001304853.1:n.1942-83T>C