Canonical Allele Identifier: CA2184198241
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66703261G= , CM000677.2:g.66703261G= GRCh38
NC_000015.9:g.66995599G= , CM000677.1:g.66995599G= GRCh37
NC_000015.8:g.64782653G= NCBI36
NG_012244.1:g.5926G=
NG_012244.2:g.5926G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.3G= MANE Select ENSP00000288840.5:p.Met1=
ENST00000288840.9:c.3G= ENSP00000288840.5:p.Met1=
ENST00000557916.5:c.3G= ENSP00000452955.1:p.Met1=
ENST00000612349.1:n.185G=
NM_005585.4:c.3G= NP_005576.3:p.Met1=
NR_027654.1:n.926G=
XR_931825.1:n.1162G=
XR_931826.1:n.1162G=
XR_931827.1:n.1162G=
XR_931827.2:n.1152G=
NM_005585.5:c.3G= MANE Select NP_005576.3:p.Met1=
NR_027654.2:n.1026G=