Canonical Allele Identifier: CA2184198198
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703219A= , CM000677.2:g.66703219A= GRCh38
NC_000015.9:g.66995557A= , CM000677.1:g.66995557A= GRCh37
NC_000015.8:g.64782611A= NCBI36
NG_012244.1:g.5884A=
NG_012244.2:g.5884A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.-40A= MANE Select ENSP00000288840.5:n.-40A=
ENST00000288840.9:c.-40A= ENSP00000288840.5:n.-40A=
ENST00000612349.1:n.143A=
NM_005585.4:c.-40A= NP_005576.3:n.-40A=
NR_027654.1:n.884A=
XR_931825.1:n.1120A=
XR_931826.1:n.1120A=
XR_931827.1:n.1120A=
XR_931827.2:n.1110A=
NM_005585.5:c.-40A= MANE Select NP_005576.3:n.-40A=
NR_027654.2:n.984A=