Canonical Allele Identifier: CA1671216779
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795914T= , CM000668.2:g.147795914T= GRCh38
NC_000006.11:g.148117050T= , CM000668.1:g.148117050T= GRCh37
NC_000006.10:g.148158743T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151558T= XP_016866339.1:n.460-151558T=