Canonical Allele Identifier: CA1095587919
Gene: SAMD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796027T>A , CM000668.2:g.147796027T>A GRCh38
NC_000006.11:g.148117163T>A , CM000668.1:g.148117163T>A GRCh37
NC_000006.10:g.148158856T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151445T>A XP_016866339.1:n.460-151445T>A