Canonical Allele Identifier: CA1095587828
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792684481

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795995A>C , CM000668.2:g.147795995A>C GRCh38
NC_000006.11:g.148117131A>C , CM000668.1:g.148117131A>C GRCh37
NC_000006.10:g.148158824A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151477A>C XP_016866339.1:n.460-151477A>C