Canonical Allele Identifier: CA2184234607
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66780982G= , CM000677.2:g.66780982G= GRCh38
NC_000015.9:g.67073320G= , CM000677.1:g.67073320G= GRCh37
NC_000015.8:g.64860374G= NCBI36
NG_012244.1:g.83647G=
NG_012244.2:g.83647G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.953-15G= MANE Select ENSP00000288840.5:n.953-15G=
ENST00000288840.9:c.953-15G= ENSP00000288840.5:n.953-15G=
ENST00000557916.5:c.1085-15G= ENSP00000452955.1:n.1085-15G=
ENST00000559931.5:c.257-15G= ENSP00000453446.1:n.257-15G=
NM_005585.4:c.953-15G= NP_005576.3:n.953-15G=
NR_027654.1:n.2008-15G=
XM_011521561.1:c.170-15G= XP_011519863.1:n.170-15G=
XR_931825.1:n.2352-15G=
XM_011521561.2:c.170-15G= XP_011519863.1:n.170-15G=
NM_005585.5:c.953-15G= MANE Select NP_005576.3:n.953-15G=
NR_027654.2:n.2108-15G=