Canonical Allele Identifier: CA2184368492
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67065899T= , CM000677.2:g.67065899T= GRCh38
NC_000015.9:g.67358237T= , CM000677.1:g.67358237T= GRCh37
NC_000015.8:g.65145291T= NCBI36
NG_011990.1:g.5043T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+1955T= ENSP00000453082.2:n.-110+1955T=
ENST00000560424.2:c.-256T= ENSP00000455540.2:n.-256T=
ENST00000327367.9:c.-256T= MANE Select ENSP00000332973.4:n.-256T=
ENST00000327367.8:c.-256T= ENSP00000332973.4:n.-256T=
ENST00000559460.5:c.-110+1955T= ENSP00000453082.1:n.-110+1955T=
NM_005902.3:c.-256T= NP_005893.1:n.-256T=
XM_011521559.1:c.-256T= XP_011519861.1:n.-256T=
NM_005902.4:c.-256T= MANE Select NP_005893.1:n.-256T=