Canonical Allele Identifier: CA917882763
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1562375872

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795917_147795920del , CM000668.2:g.147795917_147795920del GRCh38
NC_000006.11:g.148117053_148117056del , CM000668.1:g.148117053_148117056del GRCh37
NC_000006.10:g.148158746_148158749del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151555_460-151552del XP_016866339.1:n.460-151555_460-151552del