Canonical Allele Identifier: CA2184198165
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703170G= , CM000677.2:g.66703170G= GRCh38
NC_000015.9:g.66995508G= , CM000677.1:g.66995508G= GRCh37
NC_000015.8:g.64782562G= NCBI36
NG_012244.1:g.5835G=
NG_012244.2:g.5835G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.-89G= MANE Select ENSP00000288840.5:n.-89G=
ENST00000288840.9:c.-89G= ENSP00000288840.5:n.-89G=
ENST00000612349.1:n.94G=
NM_005585.4:c.-89G= NP_005576.3:n.-89G=
NR_027654.1:n.835G=
XR_931825.1:n.1071G=
XR_931826.1:n.1071G=
XR_931827.1:n.1071G=
XR_931827.2:n.1061G=
NM_005585.5:c.-89G= MANE Select NP_005576.3:n.-89G=
NR_027654.2:n.935G=