Canonical Allele Identifier: CA1671134944
Community Standard Title: NC_000006.12:g.147613811G=
Gene: SAMD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.147613811G= , CM000668.2:g.147613811G= GRCh38
NC_000006.11:g.147934947G= , CM000668.1:g.147934947G= GRCh37
NC_000006.10:g.147976640G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000566741.1:c.162+104424G= ENSP00000456528.1:n.162+104424G=
XM_011535819.1:c.459+104424G= XP_011534121.1:n.459+104424G=
XM_017010850.1:c.459+104424G= XP_016866339.1:n.459+104424G=