Canonical Allele Identifier: CA16614552
Gene: SMAD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 405561
dbSNP Id: rs1060500766

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67187473G>A , CM000677.2:g.67187473G>A GRCh38
NC_000015.9:g.67479811G>A , CM000677.1:g.67479811G>A GRCh37
NC_000015.8:g.65266865G>A NCBI36
NG_011990.1:g.126617G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558428.6:c.533G>A ENSP00000454165.2:p.Arg178His
ENST00000558739.2:c.803G>A ENSP00000453684.2:p.Arg268His
ENST00000558827.2:c.533G>A ENSP00000452767.2:p.Arg178His
ENST00000559460.6:c.803G>A ENSP00000453082.2:p.Arg268His
ENST00000560424.2:c.1229G>A ENSP00000455540.2:p.Arg410His
ENST00000327367.9:c.1118G>A MANE Select ENSP00000332973.4:p.Arg373His
ENST00000679624.1:c.803G>A ENSP00000505445.1:p.Arg268His
ENST00000680689.1:n.821G>A
ENST00000681239.1:c.803G>A ENSP00000505641.1:p.Arg268His
ENST00000327367.8:c.1118G>A ENSP00000332973.4:p.Arg373His
ENST00000439724.7:c.986G>A ENSP00000401133.3:p.Arg329His
ENST00000537194.6:c.533G>A ENSP00000445348.2:p.Arg178His
ENST00000540846.6:c.803G>A ENSP00000437757.2:p.Arg268His
ENST00000558763.1:n.812G>A
ENST00000560402.1:n.283-5400G>A
ENST00000560424.1:c.310G>A
NM_001145102.1:c.803G>A NP_001138574.1:p.Arg268His
NM_001145103.1:c.986G>A NP_001138575.1:p.Arg329His
NM_001145104.1:c.533G>A NP_001138576.1:p.Arg178His
NM_005902.3:c.1118G>A NP_005893.1:p.Arg373His
XM_011521559.1:c.986G>A XP_011519861.1:p.Arg329His
XM_011521560.1:c.971G>A XP_011519862.1:p.Arg324His
XM_011521559.3:c.986G>A XP_011519861.1:p.Arg329His
NM_005902.4:c.1118G>A MANE Select NP_005893.1:p.Arg373His
NM_001145102.2:c.803G>A NP_001138574.1:p.Arg268His
NM_001145103.2:c.986G>A NP_001138575.1:p.Arg329His
NM_001145104.2:c.533G>A NP_001138576.1:p.Arg178His