Canonical Allele Identifier: CA1671216628
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1206614022
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795675C>A , CM000668.2:g.147795675C>A GRCh38
NC_000006.11:g.148116811C>A , CM000668.1:g.148116811C>A GRCh37
NC_000006.10:g.148158504C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151797C>A XP_016866339.1:n.460-151797C>A
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