Canonical Allele Identifier: CA2184368728
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066058G= , CM000677.2:g.67066058G= GRCh38
NC_000015.9:g.67358396G= , CM000677.1:g.67358396G= GRCh37
NC_000015.8:g.65145450G= NCBI36
NG_011990.1:g.5202G=

Transcript Alleles

HGVS Amino-acid change
ENST00000559460.6:c.-110+2114G= ENSP00000453082.2:n.-110+2114G=
ENST00000560424.2:c.-97G= ENSP00000455540.2:n.-97G=
ENST00000327367.9:c.-97G= MANE Select ENSP00000332973.4:n.-97G=
ENST00000327367.8:c.-97G= ENSP00000332973.4:n.-97G=
ENST00000559460.5:c.-110+2114G= ENSP00000453082.1:n.-110+2114G=
NM_005902.3:c.-97G= NP_005893.1:n.-97G=
XM_011521559.1:c.-97G= XP_011519861.1:n.-97G=
NM_005902.4:c.-97G= MANE Select NP_005893.1:n.-97G=