Canonical Allele Identifier: CA590972141

Gene: WDR37

Linked Data

• dbSNP Id: rs1255206264
• gnomAD v2: 10-1156095-T-G
• gnomAD v3: 10-1110155-T-G
• gnomAD v4: 10-1110155-T-G
• MyVariant Identifiers: chr10:g.1156095T>G (hg19) ; chr10:g.1110155T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1110155T>G , CM000672.2:g.1110155T>G	GRCh38
NC_000010.10:g.1156095T>G , CM000672.1:g.1156095T>G	GRCh37
NC_000010.9:g.1146095T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436154.2:c.1007+4888T>G	ENSP00000404346.2:n.1007+4888T>G
ENST00000704638.1:c.995+4888T>G	ENSP00000515969.1:n.995+4888T>G
ENST00000704657.1:c.*946+4888T>G	ENSP00000515982.1:n.*946+4888T>G
ENST00000704658.1:c.-89+4888T>G	ENSP00000515983.1:n.-89+4888T>G
ENST00000704671.1:n.2011+4914T>G
ENST00000704672.1:c.1080+4914T>G	ENSP00000515985.1:n.1080+4914T>G
ENST00000704673.1:c.1106+4888T>G	ENSP00000515986.1:n.1106+4888T>G
ENST00000704674.1:c.-89+4888T>G	ENSP00000515987.1:n.-89+4888T>G
ENST00000704675.1:n.512+4888T>G
ENST00000704738.1:n.1064+4914T>G
ENST00000704739.1:c.738+4888T>G
ENST00000263150.9:c.1103+4888T>G MANE Select	ENSP00000263150.4:n.1103+4888T>G
ENST00000650072.1:c.1349+4888T>G	ENSP00000497597.1:n.1349+4888T>G
ENST00000263150.8:c.1103+4888T>G	ENSP00000263150.4:n.1103+4888T>G
ENST00000358220.5:c.1103+4888T>G	ENSP00000350954.1:n.1103+4888T>G
NM_014023.3:c.1103+4888T>G	NP_054742.2:n.1103+4888T>G
NM_014023.4:c.1103+4888T>G MANE Select	NP_054742.2:n.1103+4888T>G