Canonical Allele Identifier: CA149529090
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs531926337

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795918T>C , CM000668.2:g.147795918T>C GRCh38
NC_000006.11:g.148117054T>C , CM000668.1:g.148117054T>C GRCh37
NC_000006.10:g.148158747T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151554T>C XP_016866339.1:n.460-151554T>C