Canonical Allele Identifier: CA3365869
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs773012775

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118972G>A , CM000667.2:g.111118972G>A GRCh38
NC_000005.9:g.110454670G>A , CM000667.1:g.110454670G>A GRCh37
NC_000005.8:g.110482569G>A NCBI36
NG_008979.1:g.31801G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-41G>A MANE Select ENSP00000424628.3:n.1797-41G>A
ENST00000506538.6:c.1965-41G>A ENSP00000423067.2:n.1965-41G>A
ENST00000513710.3:c.1797-41G>A ENSP00000424628.3:n.1797-41G>A
ENST00000612402.4:c.1965-41G>A ENSP00000479950.1:n.1965-41G>A
NM_139281.2:c.1965-41G>A NP_644810.1:n.1965-41G>A
XM_011543163.1:c.1965-41G>A XP_011541465.1:n.1965-41G>A
NM_139281.3:c.1797-41G>A MANE Select NP_644810.2:n.1797-41G>A