Canonical Allele Identifier: CA2184198240
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703260T= , CM000677.2:g.66703260T= GRCh38
NC_000015.9:g.66995598T= , CM000677.1:g.66995598T= GRCh37
NC_000015.8:g.64782652T= NCBI36
NG_012244.1:g.5925T=
NG_012244.2:g.5925T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.2T= MANE Select ENSP00000288840.5:p.Met1=
ENST00000288840.9:c.2T= ENSP00000288840.5:p.Met1=
ENST00000557916.5:c.2T= ENSP00000452955.1:p.Met1=
ENST00000612349.1:n.184T=
NM_005585.4:c.2T= NP_005576.3:p.Met1=
NR_027654.1:n.925T=
XR_931825.1:n.1161T=
XR_931826.1:n.1161T=
XR_931827.1:n.1161T=
XR_931827.2:n.1151T=
NM_005585.5:c.2T= MANE Select NP_005576.3:p.Met1=
NR_027654.2:n.1025T=