Canonical Allele Identifier: CA1671216786
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792683498

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795932del , CM000668.2:g.147795932del GRCh38
NC_000006.11:g.148117068del , CM000668.1:g.148117068del GRCh37
NC_000006.10:g.148158761del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151540del XP_016866339.1:n.460-151540del