Canonical Allele Identifier: CA345948679

Gene: WDR35

Linked Data

• dbSNP Id: rs1572375385
• MyVariant Identifiers: chr2:g.20189031T>G (hg19) ; chr2:g.19989270T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.19989270T>G , CM000664.2:g.19989270T>G	GRCh38
NC_000002.11:g.20189031T>G , CM000664.1:g.20189031T>G	GRCh37
NC_000002.10:g.20052512T>G	NCBI36
NG_021212.1:g.5854A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281405.9:c.37A>C MANE Select	ENSP00000281405.5:p.Asn13His
ENST00000345530.8:c.37A>C MANE Plus Clinical	ENSP00000314444.5:p.Asn13His
ENST00000281405.8:c.37A>C	ENSP00000281405.4:p.Asn13His
ENST00000345530.7:c.37A>C	ENSP00000314444.5:p.Asn13His
ENST00000414212.5:c.37A>C	ENSP00000390802.1:p.Asn13His
NM_001006657.1:c.37A>C	NP_001006658.1:p.Asn13His
NM_020779.3:c.37A>C	NP_065830.2:p.Asn13His
XR_426989.2:n.70A>C
XR_939699.1:n.70A>C
XR_001738862.1:n.70A>C
XR_426989.3:n.70A>C
XR_939699.3:n.70A>C
NM_001006657.2:c.37A>C MANE Plus Clinical	NP_001006658.1:p.Asn13His
NM_020779.4:c.37A>C MANE Select	NP_065830.2:p.Asn13His