Canonical Allele Identifier: CA1671216777
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795913G= , CM000668.2:g.147795913G= GRCh38
NC_000006.11:g.148117049G= , CM000668.1:g.148117049G= GRCh37
NC_000006.10:g.148158742G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151559G= XP_016866339.1:n.460-151559G=