Canonical Allele Identifier: CA805365318
Gene: C5orf46 HGNC NCBI

Linked Data

dbSNP Id: rs1395050071
gnomAD v3: 5-147854864-A-C
gnomAD v4: 5-147854864-A-C
MyVariant Identifiers: chr5:g.147234427A>C (hg19) chr5:g.147854864A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.147854864A>C , CM000667.2:g.147854864A>C GRCh38
NC_000005.9:g.147234427A>C , CM000667.1:g.147234427A>C GRCh37
NC_000005.8:g.147214620A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017009459.1:c.261-4322T>G XP_016864948.1:n.261-4322T>G
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