Canonical Allele Identifier: CA360613538
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119063C>A , CM000667.2:g.111119063C>A GRCh38
NC_000005.9:g.110454761C>A , CM000667.1:g.110454761C>A GRCh37
NC_000005.8:g.110482660C>A NCBI36
NG_008979.1:g.31892C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1847C>A MANE Select ENSP00000424628.3:p.Ser616Tyr
ENST00000506538.6:c.2015C>A ENSP00000423067.2:p.Ser672Tyr
ENST00000513710.3:c.1847C>A ENSP00000424628.3:p.Ser616Tyr
ENST00000612402.4:c.2015C>A ENSP00000479950.1:p.Ser672Tyr
NM_139281.2:c.2015C>A NP_644810.1:p.Ser672Tyr
XM_011543163.1:c.2015C>A XP_011541465.1:p.Ser672Tyr
NM_139281.3:c.1847C>A MANE Select NP_644810.2:p.Ser616Tyr