Canonical Allele Identifier: CA2184234721
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781142C= , CM000677.2:g.66781142C= GRCh38
NC_000015.9:g.67073480C= , CM000677.1:g.67073480C= GRCh37
NC_000015.8:g.64860534C= NCBI36
NG_012244.1:g.83807C=
NG_012244.2:g.83807C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1098C= MANE Select ENSP00000288840.5:p.Phe366=
ENST00000288840.9:c.1098C= ENSP00000288840.5:p.Phe366=
ENST00000557916.5:c.1230C= ENSP00000452955.1:n.1230C=
ENST00000559931.5:c.402C= ENSP00000453446.1:n.402C=
NM_005585.4:c.1098C= NP_005576.3:p.Phe366=
NR_027654.1:n.2153C=
XM_011521561.1:c.315C= XP_011519863.1:p.Phe105=
XR_931825.1:n.2497C=
XM_011521561.2:c.315C= XP_011519863.1:p.Phe105=
NM_005585.5:c.1098C= MANE Select NP_005576.3:p.Phe366=
NR_027654.2:n.2253C=