Canonical Allele Identifier: CA40355931
Gene: WDR64 HGNC NCBI

Linked Data

dbSNP Id: rs10926554
gnomAD v2: 1-241894086-C-A
gnomAD v3: 1-241730784-C-A
gnomAD v4: 1-241730784-C-A
MyVariant Identifiers: chr1:g.241894086C>A (hg19) chr1:g.241730784C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241730784C>A , CM000663.2:g.241730784C>A GRCh38
NC_000001.10:g.241894086C>A , CM000663.1:g.241894086C>A GRCh37
NC_000001.9:g.239960709C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000425826.3:c.1194+7348C>A ENSP00000406342.3:n.1194+7348C>A
ENST00000437684.7:c.1194+7348C>A MANE Select ENSP00000402446.4:n.1194+7348C>A
ENST00000366552.6:c.1164+7348C>A ENSP00000355510.2:n.1164+7348C>A
ENST00000414635.5:c.477+7348C>A ENSP00000406656.1:n.477+7348C>A
ENST00000437684.6:c.324+7348C>A ENSP00000402446.3:n.324+7348C>A
NM_144625.4:c.1164+7348C>A NP_653226.4:n.1164+7348C>A
XM_006711736.2:c.1194+7348C>A XP_006711799.1:n.1194+7348C>A
XM_011544084.1:c.711+7348C>A XP_011542386.1:n.711+7348C>A
XM_011544085.1:c.711+7348C>A XP_011542387.1:n.711+7348C>A
XM_011544086.1:c.711+7348C>A XP_011542388.1:n.711+7348C>A
XM_011544087.1:c.1194+7348C>A XP_011542389.1:n.1194+7348C>A
XM_011544088.1:c.255+7348C>A XP_011542390.1:n.255+7348C>A
XM_011544089.1:c.201+7348C>A XP_011542391.1:n.201+7348C>A
XM_011544090.1:c.201+7348C>A XP_011542392.1:n.201+7348C>A
XM_011544091.1:c.1194+7348C>A XP_011542393.1:n.1194+7348C>A
XM_011544092.1:c.1194+7348C>A XP_011542394.1:n.1194+7348C>A
XM_011544093.1:c.1194+7348C>A XP_011542395.1:n.1194+7348C>A
XR_949326.1:n.54-1950G>T
XM_006711736.3:c.1194+7348C>A XP_006711799.1:n.1194+7348C>A
XM_011544086.3:c.711+7348C>A XP_011542388.1:n.711+7348C>A
XM_011544087.2:c.1194+7348C>A XP_011542389.1:n.1194+7348C>A
XM_011544092.2:c.1194+7348C>A XP_011542394.1:n.1194+7348C>A
XM_017000315.1:c.942+7348C>A XP_016855804.1:n.942+7348C>A
XR_002959419.1:n.1401+7348C>A
NM_001367482.1:c.1194+7348C>A MANE Select NP_001354411.1:n.1194+7348C>A
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