Canonical Allele Identifier: CA970972678
Gene: SMAD3 HGNC NCBI

Linked Data

dbSNP Id: rs1963360468

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67191346G>A , CM000677.2:g.67191346G>A GRCh38
NC_000015.9:g.67483684G>A , CM000677.1:g.67483684G>A GRCh37
NC_000015.8:g.65270738G>A NCBI36
NG_011990.1:g.130490G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558428.6:c.*810G>A ENSP00000454165.2:n.*810G>A
ENST00000558739.2:c.*810G>A ENSP00000453684.2:n.*810G>A
ENST00000558827.2:c.*810G>A ENSP00000452767.2:n.*810G>A
ENST00000559460.6:c.*810G>A ENSP00000453082.2:n.*810G>A
ENST00000560424.2:c.*810G>A ENSP00000455540.2:n.*810G>A
ENST00000327367.9:c.*810G>A MANE Select ENSP00000332973.4:n.*810G>A
ENST00000679624.1:c.*810G>A ENSP00000505445.1:n.*810G>A
ENST00000681239.1:c.*810G>A ENSP00000505641.1:n.*810G>A
ENST00000327367.8:c.*810G>A ENSP00000332973.4:n.*810G>A
ENST00000558763.1:n.1782G>A
ENST00000560402.1:n.283-1527G>A
NM_001145102.1:c.*810G>A NP_001138574.1:n.*810G>A
NM_001145103.1:c.*810G>A NP_001138575.1:n.*810G>A
NM_001145104.1:c.*810G>A NP_001138576.1:n.*810G>A
NM_005902.3:c.*810G>A NP_005893.1:n.*810G>A
XM_011521559.1:c.*810G>A XP_011519861.1:n.*810G>A
XM_011521560.1:c.*810G>A XP_011519862.1:n.*810G>A
XM_011521559.3:c.*810G>A XP_011519861.1:n.*810G>A
NM_005902.4:c.*810G>A MANE Select NP_005893.1:n.*810G>A
NM_001145102.2:c.*810G>A NP_001138574.1:n.*810G>A
NM_001145103.2:c.*810G>A NP_001138575.1:n.*810G>A
NM_001145104.2:c.*810G>A NP_001138576.1:n.*810G>A