Canonical Allele Identifier: CA1671216660
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795732T= , CM000668.2:g.147795732T= GRCh38
NC_000006.11:g.148116868T= , CM000668.1:g.148116868T= GRCh37
NC_000006.10:g.148158561T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151740T= XP_016866339.1:n.460-151740T=