Canonical Allele Identifier: CA10613429

Gene: WDR35

Linked Data

• ClinVar Variation Id: 333340
• ClinVar RCV Id: RCV000270103 ; RCV000364671
• dbSNP Id: rs886055399
• MyVariant Identifiers: chr2:g.20111385T>C (hg19) ; chr2:g.19911624T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19911624T>C , CM000664.2:g.19911624T>C	GRCh38
NC_000002.11:g.20111385T>C , CM000664.1:g.20111385T>C	GRCh37
NC_000002.10:g.19974866T>C	NCBI36
NG_021212.1:g.83500A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.*1934A>G MANE Select	ENSP00000281405.5:n.*1934A>G
ENST00000345530.8:c.*1934A>G MANE Plus Clinical	ENSP00000314444.5:n.*1934A>G
ENST00000281405.8:c.*1934A>G	ENSP00000281405.4:n.*1934A>G
ENST00000345530.7:c.*1934A>G	ENSP00000314444.5:n.*1934A>G
NM_001006657.1:c.*1934A>G	NP_001006658.1:n.*1934A>G
NM_020779.3:c.*1934A>G	NP_065830.2:n.*1934A>G
XM_011533007.1:c.*1934A>G	XP_011531309.1:n.*1934A>G
XM_011533007.2:c.*1934A>G	XP_011531309.1:n.*1934A>G
XR_426989.3:n.5380A>G
NM_001006657.2:c.*1934A>G MANE Plus Clinical	NP_001006658.1:n.*1934A>G
NM_020779.4:c.*1934A>G MANE Select	NP_065830.2:n.*1934A>G