Canonical Allele Identifier: CA360613464
Gene: WDR36 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119028T>G , CM000667.2:g.111119028T>G GRCh38
NC_000005.9:g.110454726T>G , CM000667.1:g.110454726T>G GRCh37
NC_000005.8:g.110482625T>G NCBI36
NG_008979.1:g.31857T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1812T>G MANE Select ENSP00000424628.3:p.Phe604Leu
ENST00000506538.6:c.1980T>G ENSP00000423067.2:p.Phe660Leu
ENST00000513710.3:c.1812T>G ENSP00000424628.3:p.Phe604Leu
ENST00000612402.4:c.1980T>G ENSP00000479950.1:p.Phe660Leu
NM_139281.2:c.1980T>G NP_644810.1:p.Phe660Leu
XM_011543163.1:c.1980T>G XP_011541465.1:p.Phe660Leu
NM_139281.3:c.1812T>G MANE Select NP_644810.2:p.Phe604Leu