Canonical Allele Identifier: CA7626727
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs777149662

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66781143T>C , CM000677.2:g.66781143T>C GRCh38
NC_000015.9:g.67073481T>C , CM000677.1:g.67073481T>C GRCh37
NC_000015.8:g.64860535T>C NCBI36
NG_012244.1:g.83808T>C
NG_012244.2:g.83808T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.1099T>C MANE Select ENSP00000288840.5:p.Cys367Arg
ENST00000288840.9:c.1099T>C ENSP00000288840.5:p.Cys367Arg
ENST00000557916.5:c.1231T>C ENSP00000452955.1:n.1231T>C
ENST00000559931.5:c.403T>C ENSP00000453446.1:n.403T>C
NM_005585.4:c.1099T>C NP_005576.3:p.Cys367Arg
NR_027654.1:n.2154T>C
XM_011521561.1:c.316T>C XP_011519863.1:p.Cys106Arg
XR_931825.1:n.2498T>C
XM_011521561.2:c.316T>C XP_011519863.1:p.Cys106Arg
NM_005585.5:c.1099T>C MANE Select NP_005576.3:p.Cys367Arg
NR_027654.2:n.2254T>C