Canonical Allele Identifier: CA1663533193
Gene: SAMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.130228918C= , CM000668.2:g.130228918C= GRCh38
NC_000006.11:g.130550063C= , CM000668.1:g.130550063C= GRCh37
NC_000006.10:g.130591756C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001258275.2:c.-187-6105G= NP_001245204.1:n.-187-6105G=
NM_001258275.3:c.-187-6105G= NP_001245204.1:n.-187-6105G=
ENST00000368134.6:c.-187-6105G= ENSP00000357116.2:n.-187-6105G=
ENST00000529119.1:n.70-6105G=
XM_024446334.1:c.-187-6105G= XP_024302102.1:n.-187-6105G=
XM_024446335.1:c.-187-6105G= XP_024302103.1:n.-187-6105G=