Canonical Allele Identifier: CA1543639

Gene: WDR35

Linked Data

• dbSNP Id: rs766525923
• ExAC: 2:20188976 C / T
• gnomAD v2: 2-20188976-C-T
• gnomAD v4: 2-19989215-C-T
• MyVariant Identifiers: chr2:g.20188976C>T (hg19) ; chr2:g.19989215C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989215C>T , CM000664.2:g.19989215C>T	GRCh38
NC_000002.11:g.20188976C>T , CM000664.1:g.20188976C>T	GRCh37
NC_000002.10:g.20052457C>T	NCBI36
NG_021212.1:g.5909G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.92G>A MANE Select	ENSP00000281405.5:p.Cys31Tyr
ENST00000345530.8:c.92G>A MANE Plus Clinical	ENSP00000314444.5:p.Cys31Tyr
ENST00000281405.8:c.92G>A	ENSP00000281405.4:p.Cys31Tyr
ENST00000345530.7:c.92G>A	ENSP00000314444.5:p.Cys31Tyr
ENST00000414212.5:c.92G>A	ENSP00000390802.1:p.Cys31Tyr
NM_001006657.1:c.92G>A	NP_001006658.1:p.Cys31Tyr
NM_020779.3:c.92G>A	NP_065830.2:p.Cys31Tyr
XR_426989.2:n.125G>A
XR_939699.1:n.125G>A
XR_001738862.1:n.125G>A
XR_426989.3:n.125G>A
XR_939699.3:n.125G>A
NM_001006657.2:c.92G>A MANE Plus Clinical	NP_001006658.1:p.Cys31Tyr
NM_020779.4:c.92G>A MANE Select	NP_065830.2:p.Cys31Tyr