Canonical Allele Identifier: CA10611888

Gene: WDR35

Linked Data

• ClinVar Variation Id: 333336
• ClinVar RCV Id: RCV000298684 ; RCV000404537
• dbSNP Id: rs112569580
• gnomAD v2: 2-20110911-C-G
• gnomAD v3: 2-19911150-C-G
• gnomAD v4: 2-19911150-C-G
• MyVariant Identifiers: chr2:g.20110911C>G (hg19) ; chr2:g.19911150C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19911150C>G , CM000664.2:g.19911150C>G	GRCh38
NC_000002.11:g.20110911C>G , CM000664.1:g.20110911C>G	GRCh37
NC_000002.10:g.19974392C>G	NCBI36
NG_021212.1:g.83974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.*2408G>C MANE Select	ENSP00000281405.5:n.*2408G>C
ENST00000345530.8:c.*2408G>C MANE Plus Clinical	ENSP00000314444.5:n.*2408G>C
ENST00000281405.8:c.*2408G>C	ENSP00000281405.4:n.*2408G>C
ENST00000345530.7:c.*2408G>C	ENSP00000314444.5:n.*2408G>C
NM_001006657.1:c.*2408G>C	NP_001006658.1:n.*2408G>C
NM_020779.3:c.*2408G>C	NP_065830.2:n.*2408G>C
XM_011533007.1:c.*2408G>C	XP_011531309.1:n.*2408G>C
XM_011533007.2:c.*2408G>C	XP_011531309.1:n.*2408G>C
XR_426989.3:n.5854G>C
NM_001006657.2:c.*2408G>C MANE Plus Clinical	NP_001006658.1:n.*2408G>C
NM_020779.4:c.*2408G>C MANE Select	NP_065830.2:n.*2408G>C