Canonical Allele Identifier: CA820491992
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1373120475

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795846dup , CM000668.2:g.147795846dup GRCh38
NC_000006.11:g.148116982dup , CM000668.1:g.148116982dup GRCh37
NC_000006.10:g.148158675dup NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151626dup XP_016866339.1:n.460-151626dup