Canonical Allele Identifier: CA16618061

Gene: WDR36

Linked Data

• ClinVar Variation Id: 424172
• ClinVar RCV Id: RCV000482086
• dbSNP Id: rs1064796838
• gnomAD v4: 5-111092293-G-A
• MyVariant Identifiers: chr5:g.110427991G>A (hg19) ; chr5:g.111092293G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111092293G>A , CM000667.2:g.111092293G>A	GRCh38
NC_000005.9:g.110427991G>A , CM000667.1:g.110427991G>A	GRCh37
NC_000005.8:g.110455890G>A	NCBI36
NG_008979.1:g.5122G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506538.6:c.5G>A	ENSP00000423067.2:p.Cys2Tyr
ENST00000612402.4:c.5G>A	ENSP00000479950.1:p.Cys2Tyr
NM_139281.2:c.5G>A	NP_644810.1:p.Cys2Tyr
XM_011543163.1:c.5G>A	XP_011541465.1:p.Cys2Tyr