Canonical Allele Identifier: CA124902797

Gene: WDR36

Linked Data

• dbSNP Id: rs559940380
• MyVariant Identifiers: chr5:g.110434228T>G (hg19) ; chr5:g.111098530T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098530T>G , CM000667.2:g.111098530T>G	GRCh38
NC_000005.9:g.110434228T>G , CM000667.1:g.110434228T>G	GRCh37
NC_000005.8:g.110462127T>G	NCBI36
NG_008979.1:g.11359T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-192T>G MANE Select	ENSP00000424628.3:n.292-192T>G
ENST00000504122.2:n.174-192T>G
ENST00000505303.5:n.428-192T>G
ENST00000506538.6:c.460-192T>G	ENSP00000423067.2:n.460-192T>G
ENST00000513710.3:c.292-192T>G	ENSP00000424628.3:n.292-192T>G
ENST00000612402.4:c.460-192T>G	ENSP00000479950.1:n.460-192T>G
NM_139281.2:c.460-192T>G	NP_644810.1:n.460-192T>G
XM_011543163.1:c.460-192T>G	XP_011541465.1:n.460-192T>G
NM_139281.3:c.292-192T>G MANE Select	NP_644810.2:n.292-192T>G