Canonical Allele Identifier: CA7626730
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs750590200

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781151C>A , CM000677.2:g.66781151C>A GRCh38
NC_000015.9:g.67073489C>A , CM000677.1:g.67073489C>A GRCh37
NC_000015.8:g.64860543C>A NCBI36
NG_012244.1:g.83816C>A
NG_012244.2:g.83816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1107C>A MANE Select ENSP00000288840.5:p.Gly369=
ENST00000288840.9:c.1107C>A ENSP00000288840.5:p.Gly369=
ENST00000557916.5:c.1239C>A ENSP00000452955.1:n.1239C>A
ENST00000559931.5:c.411C>A ENSP00000453446.1:n.411C>A
NM_005585.4:c.1107C>A NP_005576.3:p.Gly369=
NR_027654.1:n.2162C>A
XM_011521561.1:c.324C>A XP_011519863.1:p.Gly108=
XR_931825.1:n.2506C>A
XM_011521561.2:c.324C>A XP_011519863.1:p.Gly108=
NM_005585.5:c.1107C>A MANE Select NP_005576.3:p.Gly369=
NR_027654.2:n.2262C>A