Canonical Allele Identifier: CA571284299
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1307258900

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795917G>A , CM000668.2:g.147795917G>A GRCh38
NC_000006.11:g.148117053G>A , CM000668.1:g.148117053G>A GRCh37
NC_000006.10:g.148158746G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151555G>A XP_016866339.1:n.460-151555G>A