Canonical Allele Identifier: CA2184374714
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67085998C= , CM000677.2:g.67085998C= GRCh38
NC_000015.9:g.67378336C= , CM000677.1:g.67378336C= GRCh37
NC_000015.8:g.65165390C= NCBI36
NG_011990.1:g.25142C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+22054C= ENSP00000453082.2:n.-110+22054C=
ENST00000560424.2:c.206+19638C= ENSP00000455540.2:n.206+19638C=
ENST00000327367.9:c.206+19638C= MANE Select ENSP00000332973.4:n.206+19638C=
ENST00000679624.1:c.-110+18085C= ENSP00000505445.1:n.-110+18085C=
ENST00000327367.8:c.206+19638C= ENSP00000332973.4:n.206+19638C=
ENST00000559460.5:c.-110+22054C= ENSP00000453082.1:n.-110+22054C=
ENST00000559937.1:n.56+7957C=
NM_005902.3:c.206+19638C= NP_005893.1:n.206+19638C=
XM_011521559.1:c.206+19638C= XP_011519861.1:n.206+19638C=
XM_011521559.3:c.206+19638C= XP_011519861.1:n.206+19638C=
NM_005902.4:c.206+19638C= MANE Select NP_005893.1:n.206+19638C=