Canonical Allele Identifier: CA561883900
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1561708969
gnomAD v2: 5-110454543-TA-T
gnomAD v3: 5-111118845-TA-T
gnomAD v4: 5-111118845-TA-T
MyVariant Identifiers: chr5:g.110454544del (hg19) chr5:g.111118846del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118847del , CM000667.2:g.111118847del GRCh38
NC_000005.9:g.110454545del , CM000667.1:g.110454545del GRCh37
NC_000005.8:g.110482444del NCBI36
NG_008979.1:g.31676del

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-166del MANE Select ENSP00000424628.3:n.1797-166del
ENST00000506538.6:c.1965-166del ENSP00000423067.2:n.1965-166del
ENST00000513710.3:c.1797-166del ENSP00000424628.3:n.1797-166del
ENST00000612402.4:c.1965-166del ENSP00000479950.1:n.1965-166del
NM_139281.2:c.1965-166del NP_644810.1:n.1965-166del
XM_011543163.1:c.1965-166del XP_011541465.1:n.1965-166del
NM_139281.3:c.1797-166del MANE Select NP_644810.2:n.1797-166del
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