Canonical Allele Identifier: CA2184234697
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781104G= , CM000677.2:g.66781104G= GRCh38
NC_000015.9:g.67073442G= , CM000677.1:g.67073442G= GRCh37
NC_000015.8:g.64860496G= NCBI36
NG_012244.1:g.83769G=
NG_012244.2:g.83769G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1060G= MANE Select ENSP00000288840.5:p.Val354=
ENST00000288840.9:c.1060G= ENSP00000288840.5:p.Val354=
ENST00000557916.5:c.1192G= ENSP00000452955.1:n.1192G=
ENST00000559931.5:c.364G= ENSP00000453446.1:n.364G=
NM_005585.4:c.1060G= NP_005576.3:p.Val354=
NR_027654.1:n.2115G=
XM_011521561.1:c.277G= XP_011519863.1:p.Val93=
XR_931825.1:n.2459G=
XM_011521561.2:c.277G= XP_011519863.1:p.Val93=
NM_005585.5:c.1060G= MANE Select NP_005576.3:p.Val354=
NR_027654.2:n.2215G=