Canonical Allele Identifier: CA1572628238
Gene: WDR36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118873T= , CM000667.2:g.111118873T= GRCh38
NC_000005.9:g.110454571T= , CM000667.1:g.110454571T= GRCh37
NC_000005.8:g.110482470T= NCBI36
NG_008979.1:g.31702T=

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-140T= MANE Select ENSP00000424628.3:n.1797-140T=
ENST00000506538.6:c.1965-140T= ENSP00000423067.2:n.1965-140T=
ENST00000513710.3:c.1797-140T= ENSP00000424628.3:n.1797-140T=
ENST00000612402.4:c.1965-140T= ENSP00000479950.1:n.1965-140T=
NM_139281.2:c.1965-140T= NP_644810.1:n.1965-140T=
XM_011543163.1:c.1965-140T= XP_011541465.1:n.1965-140T=
NM_139281.3:c.1797-140T= MANE Select NP_644810.2:n.1797-140T=