Canonical Allele Identifier: CA820491745
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1450297201
gnomAD v3: 6-147795461-A-G
gnomAD v4: 6-147795461-A-G
MyVariant Identifiers: chr6:g.148116597A>G (hg19) chr6:g.147795461A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795461A>G , CM000668.2:g.147795461A>G GRCh38
NC_000006.11:g.148116597A>G , CM000668.1:g.148116597A>G GRCh37
NC_000006.10:g.148158290A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-152011A>G XP_016866339.1:n.460-152011A>G
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