Canonical Allele Identifier: CA392953840
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67164943T>C , CM000677.2:g.67164943T>C GRCh38
NC_000015.9:g.67457281T>C , CM000677.1:g.67457281T>C GRCh37
NC_000015.8:g.65244335T>C NCBI36
NG_011990.1:g.104087T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.-61T>C ENSP00000453684.2:n.-61T>C
ENST00000559460.6:c.-61T>C ENSP00000453082.2:n.-61T>C
ENST00000560424.2:c.255T>C ENSP00000455540.2:p.His85=
ENST00000327367.9:c.255T>C MANE Select ENSP00000332973.4:p.His85=
ENST00000679624.1:c.-61T>C ENSP00000505445.1:n.-61T>C
ENST00000681239.1:c.-61T>C ENSP00000505641.1:n.-61T>C
ENST00000327367.8:c.255T>C ENSP00000332973.4:p.His85=
ENST00000439724.7:c.123T>C ENSP00000401133.3:p.His41=
ENST00000540846.6:c.-61T>C ENSP00000437757.2:n.-61T>C
ENST00000558739.1:c.-61T>C ENSP00000453684.1:n.-61T>C
ENST00000558894.5:c.-61T>C ENSP00000458060.1:n.-61T>C
ENST00000559092.1:c.200T>C ENSP00000453788.1:p.Met67Thr
ENST00000559460.5:c.-61T>C ENSP00000453082.1:n.-61T>C
ENST00000559937.1:n.105T>C
ENST00000560175.5:c.-61T>C ENSP00000455095.1:n.-61T>C
NM_001145102.1:c.-61T>C NP_001138574.1:n.-61T>C
NM_001145103.1:c.123T>C NP_001138575.1:p.His41=
NM_005902.3:c.255T>C NP_005893.1:p.His85=
XM_011521559.1:c.255T>C XP_011519861.1:p.His85=
XM_011521560.1:c.108T>C XP_011519862.1:p.His36=
XM_011521559.3:c.255T>C XP_011519861.1:p.His85=
NM_005902.4:c.255T>C MANE Select NP_005893.1:p.His85=
NM_001145102.2:c.-61T>C NP_001138574.1:n.-61T>C
NM_001145103.2:c.123T>C NP_001138575.1:p.His41=