Canonical Allele Identifier: CA3365888
Gene: WDR36 HGNC NCBI

Linked Data

ClinVar Variation Id: 350330
ClinVar RCV Id: RCV000961645
dbSNP Id: rs11956837

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119059A>G , CM000667.2:g.111119059A>G GRCh38
NC_000005.9:g.110454757A>G , CM000667.1:g.110454757A>G GRCh37
NC_000005.8:g.110482656A>G NCBI36
NG_008979.1:g.31888A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1843A>G MANE Select ENSP00000424628.3:p.Met615Val
ENST00000506538.6:c.2011A>G ENSP00000423067.2:p.Met671Val
ENST00000513710.3:c.1843A>G ENSP00000424628.3:p.Met615Val
ENST00000612402.4:c.2011A>G ENSP00000479950.1:p.Met671Val
NM_139281.2:c.2011A>G NP_644810.1:p.Met671Val
XM_011543163.1:c.2011A>G XP_011541465.1:p.Met671Val
NM_139281.3:c.1843A>G MANE Select NP_644810.2:p.Met615Val