Canonical Allele Identifier: CA149529077
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs527431916

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795822G>A , CM000668.2:g.147795822G>A GRCh38
NC_000006.11:g.148116958G>A , CM000668.1:g.148116958G>A GRCh37
NC_000006.10:g.148158651G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151650G>A XP_016866339.1:n.460-151650G>A