Canonical Allele Identifier: CA360613619
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119101C>T , CM000667.2:g.111119101C>T GRCh38
NC_000005.9:g.110454799C>T , CM000667.1:g.110454799C>T GRCh37
NC_000005.8:g.110482698C>T NCBI36
NG_008979.1:g.31930C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1885C>T MANE Select ENSP00000424628.3:p.His629Tyr
ENST00000506538.6:c.2053C>T ENSP00000423067.2:p.His685Tyr
ENST00000513710.3:c.1885C>T ENSP00000424628.3:p.His629Tyr
ENST00000612402.4:c.2053C>T ENSP00000479950.1:p.His685Tyr
NM_139281.2:c.2053C>T NP_644810.1:p.His685Tyr
XM_011543163.1:c.2053C>T XP_011541465.1:p.His685Tyr
NM_139281.3:c.1885C>T MANE Select NP_644810.2:p.His629Tyr