Canonical Allele Identifier: CA3365897
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs756480432
ExAC: 5:110454814 C / A
gnomAD v2: 5-110454814-C-A
gnomAD v4: 5-111119116-C-A
MyVariant Identifiers: chr5:g.110454814C>A (hg19) chr5:g.111119116C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119116C>A , CM000667.2:g.111119116C>A GRCh38
NC_000005.9:g.110454814C>A , CM000667.1:g.110454814C>A GRCh37
NC_000005.8:g.110482713C>A NCBI36
NG_008979.1:g.31945C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1900C>A MANE Select ENSP00000424628.3:p.Leu634Ile
ENST00000506538.6:c.2068C>A ENSP00000423067.2:p.Leu690Ile
ENST00000513710.3:c.1900C>A ENSP00000424628.3:p.Leu634Ile
ENST00000612402.4:c.2068C>A ENSP00000479950.1:p.Leu690Ile
NM_139281.2:c.2068C>A NP_644810.1:p.Leu690Ile
XM_011543163.1:c.2068C>A XP_011541465.1:p.Leu690Ile
NM_139281.3:c.1900C>A MANE Select NP_644810.2:p.Leu634Ile
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