Canonical Allele Identifier: CA124752605
Gene: FBXL17 HGNC NCBI

Linked Data

dbSNP Id: rs1048225238
gnomAD v2: 5-107281654-C-T
gnomAD v3: 5-107945953-C-T
gnomAD v4: 5-107945953-C-T
MyVariant Identifiers: chr5:g.107281654C>T (hg19) chr5:g.107945953C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107945953C>T , CM000667.2:g.107945953C>T GRCh38
NC_000005.9:g.107281654C>T , CM000667.1:g.107281654C>T GRCh37
NC_000005.8:g.107309553C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000496714.2:c.831-64774G>A
ENST00000542267.7:c.1823-64774G>A MANE Select ENSP00000437464.2:n.1823-64774G>A
ENST00000359660.9:c.629-64774G>A ENSP00000352683.4:n.629-64774G>A
ENST00000496714.1:c.629-64774G>A ENSP00000418111.1:n.629-64774G>A
ENST00000542267.5:c.1823-64774G>A ENSP00000437464.1:n.1823-64774G>A
ENST00000619412.4:c.1109-64774G>A ENSP00000481439.1:n.1109-64774G>A
NM_001163315.2:c.1823-64774G>A NP_001156787.2:n.1823-64774G>A
XM_005272048.3:c.1823-64774G>A XP_005272105.1:n.1823-64774G>A
XM_005272048.4:c.1823-64774G>A XP_005272105.1:n.1823-64774G>A
NM_001163315.3:c.1823-64774G>A MANE Select NP_001156787.2:n.1823-64774G>A
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