Canonical Allele Identifier: CA3365898
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs551231311
ExAC: 5:110454816 A / G
gnomAD v2: 5-110454816-A-G
gnomAD v3: 5-111119118-A-G
gnomAD v4: 5-111119118-A-G
MyVariant Identifiers: chr5:g.110454816A>G (hg19) chr5:g.111119118A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119118A>G , CM000667.2:g.111119118A>G GRCh38
NC_000005.9:g.110454816A>G , CM000667.1:g.110454816A>G GRCh37
NC_000005.8:g.110482715A>G NCBI36
NG_008979.1:g.31947A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000513710.4:c.1902A>G MANE Select ENSP00000424628.3:p.Leu634=
ENST00000506538.6:c.2070A>G ENSP00000423067.2:p.Leu690=
ENST00000513710.3:c.1902A>G ENSP00000424628.3:p.Leu634=
ENST00000612402.4:c.2070A>G ENSP00000479950.1:p.Leu690=
NM_139281.2:c.2070A>G NP_644810.1:p.Leu690=
XM_011543163.1:c.2070A>G XP_011541465.1:p.Leu690=
NM_139281.3:c.1902A>G MANE Select NP_644810.2:p.Leu634=
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