Canonical Allele Identifier: CA2184234622
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781000C= , CM000677.2:g.66781000C= GRCh38
NC_000015.9:g.67073338C= , CM000677.1:g.67073338C= GRCh37
NC_000015.8:g.64860392C= NCBI36
NG_012244.1:g.83665C=
NG_012244.2:g.83665C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.956C= MANE Select ENSP00000288840.5:p.Ala319=
ENST00000288840.9:c.956C= ENSP00000288840.5:p.Ala319=
ENST00000557916.5:c.1088C= ENSP00000452955.1:n.1088C=
ENST00000559931.5:c.260C= ENSP00000453446.1:n.260C=
NM_005585.4:c.956C= NP_005576.3:p.Ala319=
NR_027654.1:n.2011C=
XM_011521561.1:c.173C= XP_011519863.1:p.Ala58=
XR_931825.1:n.2355C=
XM_011521561.2:c.173C= XP_011519863.1:p.Ala58=
NM_005585.5:c.956C= MANE Select NP_005576.3:p.Ala319=
NR_027654.2:n.2111C=