Canonical Allele Identifier: CA1095587630
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792679422

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795717dup , CM000668.2:g.147795717dup GRCh38
NC_000006.11:g.148116853dup , CM000668.1:g.148116853dup GRCh37
NC_000006.10:g.148158546dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151755dup XP_016866339.1:n.460-151755dup