Canonical Allele Identifier: CA1095588119
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792687694

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796213G>A , CM000668.2:g.147796213G>A GRCh38
NC_000006.11:g.148117349G>A , CM000668.1:g.148117349G>A GRCh37
NC_000006.10:g.148159042G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151259G>A XP_016866339.1:n.460-151259G>A