Canonical Allele Identifier: CA1671216569
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792676570

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795582G>A , CM000668.2:g.147795582G>A GRCh38
NC_000006.11:g.148116718G>A , CM000668.1:g.148116718G>A GRCh37
NC_000006.10:g.148158411G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151890G>A XP_016866339.1:n.460-151890G>A