Canonical Allele Identifier: CA393201782
Gene: SMAD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781107A>T , CM000677.2:g.66781107A>T GRCh38
NC_000015.9:g.67073445A>T , CM000677.1:g.67073445A>T GRCh37
NC_000015.8:g.64860499A>T NCBI36
NG_012244.1:g.83772A>T
NG_012244.2:g.83772A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1063A>T MANE Select ENSP00000288840.5:p.Ser355Cys
ENST00000288840.9:c.1063A>T ENSP00000288840.5:p.Ser355Cys
ENST00000557916.5:c.1195A>T ENSP00000452955.1:n.1195A>T
ENST00000559931.5:c.367A>T ENSP00000453446.1:n.367A>T
NM_005585.4:c.1063A>T NP_005576.3:p.Ser355Cys
NR_027654.1:n.2118A>T
XM_011521561.1:c.280A>T XP_011519863.1:p.Ser94Cys
XR_931825.1:n.2462A>T
XM_011521561.2:c.280A>T XP_011519863.1:p.Ser94Cys
NM_005585.5:c.1063A>T MANE Select NP_005576.3:p.Ser355Cys
NR_027654.2:n.2218A>T