Canonical Allele Identifier: CA2184198313
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703355G= , CM000677.2:g.66703355G= GRCh38
NC_000015.9:g.66995693G= , CM000677.1:g.66995693G= GRCh37
NC_000015.8:g.64782747G= NCBI36
NG_012244.1:g.6020G=
NG_012244.2:g.6020G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.97G= MANE Select ENSP00000288840.5:p.Gly33=
ENST00000288840.9:c.97G= ENSP00000288840.5:p.Gly33=
ENST00000557916.5:c.97G= ENSP00000452955.1:p.Gly33=
ENST00000612349.1:n.279G=
NM_005585.4:c.97G= NP_005576.3:p.Gly33=
NR_027654.1:n.1020G=
XR_931825.1:n.1256G=
XR_931826.1:n.1256G=
XR_931827.1:n.1256G=
XR_931827.2:n.1246G=
NM_005585.5:c.97G= MANE Select NP_005576.3:p.Gly33=
NR_027654.2:n.1120G=