Canonical Allele Identifier: CA491071698
Gene: SMAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.67457607G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67165269G>A , CM000677.2:g.67165269G>A GRCh38
NC_000015.9:g.67457607G>A , CM000677.1:g.67457607G>A GRCh37
NC_000015.8:g.65244661G>A NCBI36
NG_011990.1:g.104413G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.102G>A ENSP00000453684.2:p.Leu34=
ENST00000559460.6:c.102G>A ENSP00000453082.2:p.Leu34=
ENST00000560424.2:c.417G>A ENSP00000455540.2:p.Leu139=
ENST00000327367.9:c.417G>A MANE Select ENSP00000332973.4:p.Leu139=
ENST00000679624.1:c.102G>A ENSP00000505445.1:p.Leu34=
ENST00000681239.1:c.102G>A ENSP00000505641.1:p.Leu34=
ENST00000327367.8:c.417G>A ENSP00000332973.4:p.Leu139=
ENST00000439724.7:c.285G>A ENSP00000401133.3:p.Leu95=
ENST00000540846.6:c.102G>A ENSP00000437757.2:p.Leu34=
ENST00000558739.1:c.102G>A ENSP00000453684.1:p.Leu34=
ENST00000558894.5:c.102G>A ENSP00000458060.1:p.Leu34=
ENST00000559460.5:c.102G>A ENSP00000453082.1:p.Leu34=
ENST00000559937.1:n.267G>A
ENST00000560175.5:c.102G>A ENSP00000455095.1:p.Leu34=
NM_001145102.1:c.102G>A NP_001138574.1:p.Leu34=
NM_001145103.1:c.285G>A NP_001138575.1:p.Leu95=
NM_005902.3:c.417G>A NP_005893.1:p.Leu139=
XM_011521559.1:c.400+181G>A XP_011519861.1:n.400+181G>A
XM_011521560.1:c.270G>A XP_011519862.1:p.Leu90=
XM_011521559.3:c.400+181G>A XP_011519861.1:n.400+181G>A
NM_005902.4:c.417G>A MANE Select NP_005893.1:p.Leu139=
NM_001145102.2:c.102G>A NP_001138574.1:p.Leu34=
NM_001145103.2:c.285G>A NP_001138575.1:p.Leu95=