Canonical Allele Identifier: CA1095587572
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1792676673

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795591T>C , CM000668.2:g.147795591T>C GRCh38
NC_000006.11:g.148116727T>C , CM000668.1:g.148116727T>C GRCh37
NC_000006.10:g.148158420T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017010850.1:c.460-151881T>C XP_016866339.1:n.460-151881T>C