Canonical Allele Identifier: CA360613593
Gene: WDR36 HGNC NCBI

Linked Data

gnomAD v4: 5-111119090-C-G
MyVariant Identifiers: chr5:g.110454788C>G (hg19) chr5:g.111119090C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119090C>G , CM000667.2:g.111119090C>G GRCh38
NC_000005.9:g.110454788C>G , CM000667.1:g.110454788C>G GRCh37
NC_000005.8:g.110482687C>G NCBI36
NG_008979.1:g.31919C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1874C>G MANE Select ENSP00000424628.3:p.Ser625Cys
ENST00000506538.6:c.2042C>G ENSP00000423067.2:p.Ser681Cys
ENST00000513710.3:c.1874C>G ENSP00000424628.3:p.Ser625Cys
ENST00000612402.4:c.2042C>G ENSP00000479950.1:p.Ser681Cys
NM_139281.2:c.2042C>G NP_644810.1:p.Ser681Cys
XM_011543163.1:c.2042C>G XP_011541465.1:p.Ser681Cys
NM_139281.3:c.1874C>G MANE Select NP_644810.2:p.Ser625Cys
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