Canonical Allele Identifier: CA360613433
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119014C>T , CM000667.2:g.111119014C>T GRCh38
NC_000005.9:g.110454712C>T , CM000667.1:g.110454712C>T GRCh37
NC_000005.8:g.110482611C>T NCBI36
NG_008979.1:g.31843C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1798C>T MANE Select ENSP00000424628.3:p.Leu600Phe
ENST00000506538.6:c.1966C>T ENSP00000423067.2:p.Leu656Phe
ENST00000513710.3:c.1798C>T ENSP00000424628.3:p.Leu600Phe
ENST00000612402.4:c.1966C>T ENSP00000479950.1:p.Leu656Phe
NM_139281.2:c.1966C>T NP_644810.1:p.Leu656Phe
XM_011543163.1:c.1966C>T XP_011541465.1:p.Leu656Phe
NM_139281.3:c.1798C>T MANE Select NP_644810.2:p.Leu600Phe