Canonical Allele Identifier: CA2773470683
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796245A>C , CM000668.2:g.147796245A>C GRCh38
NC_000006.11:g.148117381A>C , CM000668.1:g.148117381A>C GRCh37
NC_000006.10:g.148159074A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151227A>C XP_016866339.1:n.460-151227A>C