Canonical Allele Identifier: CA561883912
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1285571366

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118923A>G , CM000667.2:g.111118923A>G GRCh38
NC_000005.9:g.110454621A>G , CM000667.1:g.110454621A>G GRCh37
NC_000005.8:g.110482520A>G NCBI36
NG_008979.1:g.31752A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-90A>G MANE Select ENSP00000424628.3:n.1797-90A>G
ENST00000506538.6:c.1965-90A>G ENSP00000423067.2:n.1965-90A>G
ENST00000513710.3:c.1797-90A>G ENSP00000424628.3:n.1797-90A>G
ENST00000612402.4:c.1965-90A>G ENSP00000479950.1:n.1965-90A>G
NM_139281.2:c.1965-90A>G NP_644810.1:n.1965-90A>G
XM_011543163.1:c.1965-90A>G XP_011541465.1:n.1965-90A>G
NM_139281.3:c.1797-90A>G MANE Select NP_644810.2:n.1797-90A>G