Canonical Allele Identifier: CA1095588056
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792686309

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796122_147796123insGTCTAACGTTTA , CM000668.2:g.147796122_147796123insGTCTAACGTTTA GRCh38
NC_000006.11:g.148117258_148117259insGTCTAACGTTTA , CM000668.1:g.148117258_148117259insGTCTAACGTTTA GRCh37
NC_000006.10:g.148158951_148158952insGTCTAACGTTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151350_460-151349insGTCTAACGTTTA XP_016866339.1:n.460-151350_460-151349insGTCTAACGTTTA