Canonical Allele Identifier: CA805365411
Gene: C5orf46 HGNC NCBI

Linked Data

dbSNP Id: rs1277696594
MyVariant Identifiers: chr5:g.147234588A>C (hg19) chr5:g.147855025A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147855025A>C , CM000667.2:g.147855025A>C GRCh38
NC_000005.9:g.147234588A>C , CM000667.1:g.147234588A>C GRCh37
NC_000005.8:g.147214781A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017009459.1:c.261-4483T>G XP_016864948.1:n.261-4483T>G
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