Canonical Allele Identifier: CA1080095848
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs779534890
gnomAD v3: 5-111118777-C-T
gnomAD v4: 5-111118777-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118777C>T , CM000667.2:g.111118777C>T GRCh38
NC_000005.9:g.110454475C>T , CM000667.1:g.110454475C>T GRCh37
NC_000005.8:g.110482374C>T NCBI36
NG_008979.1:g.31606C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1797-236C>T MANE Select ENSP00000424628.3:n.1797-236C>T
ENST00000506538.6:c.1965-236C>T ENSP00000423067.2:n.1965-236C>T
ENST00000513710.3:c.1797-236C>T ENSP00000424628.3:n.1797-236C>T
ENST00000612402.4:c.1965-236C>T ENSP00000479950.1:n.1965-236C>T
NM_139281.2:c.1965-236C>T NP_644810.1:n.1965-236C>T
XM_011543163.1:c.1965-236C>T XP_011541465.1:n.1965-236C>T
NM_139281.3:c.1797-236C>T MANE Select NP_644810.2:n.1797-236C>T
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