Canonical Allele Identifier: CA392953917
Gene: SMAD3 HGNC NCBI

Linked Data

dbSNP Id: rs2140293929

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67164971C>A , CM000677.2:g.67164971C>A GRCh38
NC_000015.9:g.67457309C>A , CM000677.1:g.67457309C>A GRCh37
NC_000015.8:g.65244363C>A NCBI36
NG_011990.1:g.104115C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000558739.2:c.-33C>A ENSP00000453684.2:n.-33C>A
ENST00000559460.6:c.-33C>A ENSP00000453082.2:n.-33C>A
ENST00000560424.2:c.283C>A ENSP00000455540.2:p.Pro95Thr
ENST00000327367.9:c.283C>A MANE Select ENSP00000332973.4:p.Pro95Thr
ENST00000679624.1:c.-33C>A ENSP00000505445.1:n.-33C>A
ENST00000681239.1:c.-33C>A ENSP00000505641.1:n.-33C>A
ENST00000327367.8:c.283C>A ENSP00000332973.4:p.Pro95Thr
ENST00000439724.7:c.151C>A ENSP00000401133.3:p.Pro51Thr
ENST00000540846.6:c.-33C>A ENSP00000437757.2:n.-33C>A
ENST00000558739.1:c.-33C>A ENSP00000453684.1:n.-33C>A
ENST00000558894.5:c.-33C>A ENSP00000458060.1:n.-33C>A
ENST00000559092.1:c.228C>A ENSP00000453788.1:p.Gly76=
ENST00000559460.5:c.-33C>A ENSP00000453082.1:n.-33C>A
ENST00000559937.1:n.133C>A
ENST00000560175.5:c.-33C>A ENSP00000455095.1:n.-33C>A
NM_001145102.1:c.-33C>A NP_001138574.1:n.-33C>A
NM_001145103.1:c.151C>A NP_001138575.1:p.Pro51Thr
NM_005902.3:c.283C>A NP_005893.1:p.Pro95Thr
XM_011521559.1:c.283C>A XP_011519861.1:p.Pro95Thr
XM_011521560.1:c.136C>A XP_011519862.1:p.Pro46Thr
XM_011521559.3:c.283C>A XP_011519861.1:p.Pro95Thr
NM_005902.4:c.283C>A MANE Select NP_005893.1:p.Pro95Thr
NM_001145102.2:c.-33C>A NP_001138574.1:n.-33C>A
NM_001145103.2:c.151C>A NP_001138575.1:p.Pro51Thr