Canonical Allele Identifier: CA393201835
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs1186864526

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781132G>A , CM000677.2:g.66781132G>A GRCh38
NC_000015.9:g.67073470G>A , CM000677.1:g.67073470G>A GRCh37
NC_000015.8:g.64860524G>A NCBI36
NG_012244.1:g.83797G>A
NG_012244.2:g.83797G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1088G>A MANE Select ENSP00000288840.5:p.Gly363Asp
ENST00000288840.9:c.1088G>A ENSP00000288840.5:p.Gly363Asp
ENST00000557916.5:c.1220G>A ENSP00000452955.1:n.1220G>A
ENST00000559931.5:c.392G>A ENSP00000453446.1:n.392G>A
NM_005585.4:c.1088G>A NP_005576.3:p.Gly363Asp
NR_027654.1:n.2143G>A
XM_011521561.1:c.305G>A XP_011519863.1:p.Gly102Asp
XR_931825.1:n.2487G>A
XM_011521561.2:c.305G>A XP_011519863.1:p.Gly102Asp
NM_005585.5:c.1088G>A MANE Select NP_005576.3:p.Gly363Asp
NR_027654.2:n.2243G>A