Canonical Allele Identifier: CA3365887
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs547578412
ExAC: 5:110454755 C / T
gnomAD v2: 5-110454755-C-T
gnomAD v3: 5-111119057-C-T
gnomAD v4: 5-111119057-C-T
MyVariant Identifiers: chr5:g.110454755C>T (hg19) chr5:g.111119057C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119057C>T , CM000667.2:g.111119057C>T GRCh38
NC_000005.9:g.110454755C>T , CM000667.1:g.110454755C>T GRCh37
NC_000005.8:g.110482654C>T NCBI36
NG_008979.1:g.31886C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1841C>T MANE Select ENSP00000424628.3:p.Ser614Phe
ENST00000506538.6:c.2009C>T ENSP00000423067.2:p.Ser670Phe
ENST00000513710.3:c.1841C>T ENSP00000424628.3:p.Ser614Phe
ENST00000612402.4:c.2009C>T ENSP00000479950.1:p.Ser670Phe
NM_139281.2:c.2009C>T NP_644810.1:p.Ser670Phe
XM_011543163.1:c.2009C>T XP_011541465.1:p.Ser670Phe
NM_139281.3:c.1841C>T MANE Select NP_644810.2:p.Ser614Phe
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