Canonical Allele Identifier: CA1671216976
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792688797

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796284T>C , CM000668.2:g.147796284T>C GRCh38
NC_000006.11:g.148117420T>C , CM000668.1:g.148117420T>C GRCh37
NC_000006.10:g.148159113T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151188T>C XP_016866339.1:n.460-151188T>C