Canonical Allele Identifier: CA805365412
Gene: C5orf46 HGNC NCBI

Linked Data

dbSNP Id: rs1233064299
gnomAD v3: 5-147855029-T-A
gnomAD v4: 5-147855029-T-A
MyVariant Identifiers: chr5:g.147234592T>A (hg19) chr5:g.147855029T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147855029T>A , CM000667.2:g.147855029T>A GRCh38
NC_000005.9:g.147234592T>A , CM000667.1:g.147234592T>A GRCh37
NC_000005.8:g.147214785T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017009459.1:c.261-4487A>T XP_016864948.1:n.261-4487A>T
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