Canonical Allele Identifier: CA820491980
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1201941914

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795821G>T , CM000668.2:g.147795821G>T GRCh38
NC_000006.11:g.148116957G>T , CM000668.1:g.148116957G>T GRCh37
NC_000006.10:g.148158650G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151651G>T XP_016866339.1:n.460-151651G>T