Canonical Allele Identifier: CA345947435

Gene: WDR35

Linked Data

• ClinVar Variation Id: 2139899
• ClinVar RCV Id: RCV003052838
• MyVariant Identifiers: chr2:g.20175289A>C (hg19) ; chr2:g.19975528A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19975528A>C , CM000664.2:g.19975528A>C	GRCh38
NC_000002.11:g.20175289A>C , CM000664.1:g.20175289A>C	GRCh37
NC_000002.10:g.20038770A>C	NCBI36
NG_021212.1:g.19596T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.570+2T>G MANE Select	ENSP00000281405.5:n.570+2T>G
ENST00000345530.8:c.570+2T>G MANE Plus Clinical	ENSP00000314444.5:n.570+2T>G
ENST00000281405.8:c.570+2T>G	ENSP00000281405.4:n.570+2T>G
ENST00000345530.7:c.570+2T>G	ENSP00000314444.5:n.570+2T>G
ENST00000414212.5:c.570+2T>G	ENSP00000390802.1:n.570+2T>G
ENST00000445063.5:c.107+2T>G
NM_001006657.1:c.570+2T>G	NP_001006658.1:n.570+2T>G
NM_020779.3:c.570+2T>G	NP_065830.2:n.570+2T>G
XR_426989.2:n.603+2T>G
XR_939699.1:n.603+2T>G
XR_001738862.1:n.603+2T>G
XR_426989.3:n.603+2T>G
XR_939699.3:n.603+2T>G
NM_001006657.2:c.570+2T>G MANE Plus Clinical	NP_001006658.1:n.570+2T>G
NM_020779.4:c.570+2T>G MANE Select	NP_065830.2:n.570+2T>G