Canonical Allele Identifier: CA820491983
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1274645308

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795823T>C , CM000668.2:g.147795823T>C GRCh38
NC_000006.11:g.148116959T>C , CM000668.1:g.148116959T>C GRCh37
NC_000006.10:g.148158652T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151649T>C XP_016866339.1:n.460-151649T>C