Canonical Allele Identifier: CA360613550
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119069C>T , CM000667.2:g.111119069C>T GRCh38
NC_000005.9:g.110454767C>T , CM000667.1:g.110454767C>T GRCh37
NC_000005.8:g.110482666C>T NCBI36
NG_008979.1:g.31898C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1853C>T MANE Select ENSP00000424628.3:p.Thr618Ile
ENST00000506538.6:c.2021C>T ENSP00000423067.2:p.Thr674Ile
ENST00000513710.3:c.1853C>T ENSP00000424628.3:p.Thr618Ile
ENST00000612402.4:c.2021C>T ENSP00000479950.1:p.Thr674Ile
NM_139281.2:c.2021C>T NP_644810.1:p.Thr674Ile
XM_011543163.1:c.2021C>T XP_011541465.1:p.Thr674Ile
NM_139281.3:c.1853C>T MANE Select NP_644810.2:p.Thr618Ile