Canonical Allele Identifier: CA801886281
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1245369862
gnomAD v3: 5-111118901-G-C
gnomAD v4: 5-111118901-G-C
MyVariant Identifiers: chr5:g.110454599G>C (hg19) chr5:g.111118901G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118901G>C , CM000667.2:g.111118901G>C GRCh38
NC_000005.9:g.110454599G>C , CM000667.1:g.110454599G>C GRCh37
NC_000005.8:g.110482498G>C NCBI36
NG_008979.1:g.31730G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1797-112G>C MANE Select ENSP00000424628.3:n.1797-112G>C
ENST00000506538.6:c.1965-112G>C ENSP00000423067.2:n.1965-112G>C
ENST00000513710.3:c.1797-112G>C ENSP00000424628.3:n.1797-112G>C
ENST00000612402.4:c.1965-112G>C ENSP00000479950.1:n.1965-112G>C
NM_139281.2:c.1965-112G>C NP_644810.1:n.1965-112G>C
XM_011543163.1:c.1965-112G>C XP_011541465.1:n.1965-112G>C
NM_139281.3:c.1797-112G>C MANE Select NP_644810.2:n.1797-112G>C
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