Canonical Allele Identifier: CA1572614446
Gene: WDR36 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111098552T= , CM000667.2:g.111098552T= GRCh38
NC_000005.9:g.110434250T= , CM000667.1:g.110434250T= GRCh37
NC_000005.8:g.110462149T= NCBI36
NG_008979.1:g.11381T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.292-170T= MANE Select ENSP00000424628.3:n.292-170T=
ENST00000504122.2:n.174-170T=
ENST00000505303.5:n.428-170T=
ENST00000506538.6:c.460-170T= ENSP00000423067.2:n.460-170T=
ENST00000513710.3:c.292-170T= ENSP00000424628.3:n.292-170T=
ENST00000612402.4:c.460-170T= ENSP00000479950.1:n.460-170T=
NM_139281.2:c.460-170T= NP_644810.1:n.460-170T=
XM_011543163.1:c.460-170T= XP_011541465.1:n.460-170T=
NM_139281.3:c.292-170T= MANE Select NP_644810.2:n.292-170T=
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