Canonical Allele Identifier: CA1095588090
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792686684

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147796138G>C , CM000668.2:g.147796138G>C GRCh38
NC_000006.11:g.148117274G>C , CM000668.1:g.148117274G>C GRCh37
NC_000006.10:g.148158967G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151334G>C XP_016866339.1:n.460-151334G>C