Canonical Allele Identifier: CA393201783
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781108G>C , CM000677.2:g.66781108G>C GRCh38
NC_000015.9:g.67073446G>C , CM000677.1:g.67073446G>C GRCh37
NC_000015.8:g.64860500G>C NCBI36
NG_012244.1:g.83773G>C
NG_012244.2:g.83773G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1064G>C MANE Select ENSP00000288840.5:p.Ser355Thr
ENST00000288840.9:c.1064G>C ENSP00000288840.5:p.Ser355Thr
ENST00000557916.5:c.1196G>C ENSP00000452955.1:n.1196G>C
ENST00000559931.5:c.368G>C ENSP00000453446.1:n.368G>C
NM_005585.4:c.1064G>C NP_005576.3:p.Ser355Thr
NR_027654.1:n.2119G>C
XM_011521561.1:c.281G>C XP_011519863.1:p.Ser94Thr
XR_931825.1:n.2463G>C
XM_011521561.2:c.281G>C XP_011519863.1:p.Ser94Thr
NM_005585.5:c.1064G>C MANE Select NP_005576.3:p.Ser355Thr
NR_027654.2:n.2219G>C