Canonical Allele Identifier: CA2508704101
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795940G>A , CM000668.2:g.147795940G>A GRCh38
NC_000006.11:g.148117076G>A , CM000668.1:g.148117076G>A GRCh37
NC_000006.10:g.148158769G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151532G>A XP_016866339.1:n.460-151532G>A