Canonical Allele Identifier: CA1095587683
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792680780

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795800A>C , CM000668.2:g.147795800A>C GRCh38
NC_000006.11:g.148116936A>C , CM000668.1:g.148116936A>C GRCh37
NC_000006.10:g.148158629A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151672A>C XP_016866339.1:n.460-151672A>C