Canonical Allele Identifier: CA2184231489
Gene: SMAD6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66774134T= , CM000677.2:g.66774134T= GRCh38
NC_000015.9:g.67066472T= , CM000677.1:g.67066472T= GRCh37
NC_000015.8:g.64853526T= NCBI36
NG_012244.1:g.76799T=
NG_012244.2:g.76799T=

Transcript Alleles

HGVS Amino-acid change
ENST00000288840.10:c.953-6863T= MANE Select ENSP00000288840.5:n.953-6863T=
ENST00000288840.9:c.953-6863T= ENSP00000288840.5:n.953-6863T=
ENST00000557916.5:c.1085-6863T= ENSP00000452955.1:n.1085-6863T=
ENST00000559931.5:c.257-6863T= ENSP00000453446.1:n.257-6863T=
NM_005585.4:c.953-6863T= NP_005576.3:n.953-6863T=
NR_027654.1:n.2008-6863T=
XM_011521561.1:c.170-6863T= XP_011519863.1:n.170-6863T=
XR_931825.1:n.2352-6863T=
XM_011521561.2:c.170-6863T= XP_011519863.1:n.170-6863T=
NM_005585.5:c.953-6863T= MANE Select NP_005576.3:n.953-6863T=
NR_027654.2:n.2108-6863T=