Canonical Allele Identifier: CA1671216776
Gene: SAMD5 HGNC NCBI

Linked Data

dbSNP Id: rs1583175771

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147795912T>A , CM000668.2:g.147795912T>A GRCh38
NC_000006.11:g.148117048T>A , CM000668.1:g.148117048T>A GRCh37
NC_000006.10:g.148158741T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017010850.1:c.460-151560T>A XP_016866339.1:n.460-151560T>A