Canonical Allele Identifier: CA1543641

Gene: WDR35

Linked Data

• ClinVar Variation Id: 2927840
• ClinVar RCV Id: RCV003784470
• dbSNP Id: rs202189893
• ExAC: 2:20188978 T / C
• gnomAD v2: 2-20188978-T-C
• gnomAD v3: 2-19989217-T-C
• gnomAD v4: 2-19989217-T-C
• MyVariant Identifiers: chr2:g.20188978T>C (hg19) ; chr2:g.19989217T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989217T>C , CM000664.2:g.19989217T>C	GRCh38
NC_000002.11:g.20188978T>C , CM000664.1:g.20188978T>C	GRCh37
NC_000002.10:g.20052459T>C	NCBI36
NG_021212.1:g.5907A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.90A>G MANE Select	ENSP00000281405.5:p.Ala30=
ENST00000345530.8:c.90A>G MANE Plus Clinical	ENSP00000314444.5:p.Ala30=
ENST00000281405.8:c.90A>G	ENSP00000281405.4:p.Ala30=
ENST00000345530.7:c.90A>G	ENSP00000314444.5:p.Ala30=
ENST00000414212.5:c.90A>G	ENSP00000390802.1:p.Ala30=
NM_001006657.1:c.90A>G	NP_001006658.1:p.Ala30=
NM_020779.3:c.90A>G	NP_065830.2:p.Ala30=
XR_426989.2:n.123A>G
XR_939699.1:n.123A>G
XR_001738862.1:n.123A>G
XR_426989.3:n.123A>G
XR_939699.3:n.123A>G
NM_001006657.2:c.90A>G MANE Plus Clinical	NP_001006658.1:p.Ala30=
NM_020779.4:c.90A>G MANE Select	NP_065830.2:p.Ala30=