Canonical Allele Identifier: CA2184198295
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703337A= , CM000677.2:g.66703337A= GRCh38
NC_000015.9:g.66995675A= , CM000677.1:g.66995675A= GRCh37
NC_000015.8:g.64782729A= NCBI36
NG_012244.1:g.6002A=
NG_012244.2:g.6002A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.79A= MANE Select ENSP00000288840.5:p.Ser27=
ENST00000288840.9:c.79A= ENSP00000288840.5:p.Ser27=
ENST00000557916.5:c.79A= ENSP00000452955.1:p.Ser27=
ENST00000612349.1:n.261A=
NM_005585.4:c.79A= NP_005576.3:p.Ser27=
NR_027654.1:n.1002A=
XR_931825.1:n.1238A=
XR_931826.1:n.1238A=
XR_931827.1:n.1238A=
XR_931827.2:n.1228A=
NM_005585.5:c.79A= MANE Select NP_005576.3:p.Ser27=
NR_027654.2:n.1102A=