Canonical Allele Identifier: CA1671216767
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795903T= , CM000668.2:g.147795903T= GRCh38
NC_000006.11:g.148117039T= , CM000668.1:g.148117039T= GRCh37
NC_000006.10:g.148158732T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151569T= XP_016866339.1:n.460-151569T=