Canonical Allele Identifier: CA1095587898
Gene: SAMD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796018C>T , CM000668.2:g.147796018C>T GRCh38
NC_000006.11:g.148117154C>T , CM000668.1:g.148117154C>T GRCh37
NC_000006.10:g.148158847C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151454C>T XP_016866339.1:n.460-151454C>T