Canonical Allele Identifier: CA392954302

Gene: SMAD3

Linked Data

• dbSNP Id: rs1595942172
• MyVariant Identifiers: chr15:g.67457627T>C (hg19) ; chr15:g.67165289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67165289T>C , CM000677.2:g.67165289T>C	GRCh38
NC_000015.9:g.67457627T>C , CM000677.1:g.67457627T>C	GRCh37
NC_000015.8:g.65244681T>C	NCBI36
NG_011990.1:g.104433T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.122T>C	ENSP00000453684.2:p.Ile41Thr
ENST00000559460.6:c.122T>C	ENSP00000453082.2:p.Ile41Thr
ENST00000560424.2:c.437T>C	ENSP00000455540.2:p.Ile146Thr
ENST00000327367.9:c.437T>C MANE Select	ENSP00000332973.4:p.Ile146Thr
ENST00000679624.1:c.122T>C	ENSP00000505445.1:p.Ile41Thr
ENST00000681239.1:c.122T>C	ENSP00000505641.1:p.Ile41Thr
ENST00000327367.8:c.437T>C	ENSP00000332973.4:p.Ile146Thr
ENST00000439724.7:c.305T>C	ENSP00000401133.3:p.Ile102Thr
ENST00000540846.6:c.122T>C	ENSP00000437757.2:p.Ile41Thr
ENST00000558739.1:c.122T>C	ENSP00000453684.1:p.Ile41Thr
ENST00000558894.5:c.122T>C	ENSP00000458060.1:p.Ile41Thr
ENST00000559460.5:c.122T>C	ENSP00000453082.1:p.Ile41Thr
ENST00000559937.1:n.287T>C
ENST00000560175.5:c.122T>C	ENSP00000455095.1:p.Ile41Thr
NM_001145102.1:c.122T>C	NP_001138574.1:p.Ile41Thr
NM_001145103.1:c.305T>C	NP_001138575.1:p.Ile102Thr
NM_005902.3:c.437T>C	NP_005893.1:p.Ile146Thr
XM_011521559.1:c.400+201T>C	XP_011519861.1:n.400+201T>C
XM_011521560.1:c.290T>C	XP_011519862.1:p.Ile97Thr
XM_011521559.3:c.400+201T>C	XP_011519861.1:n.400+201T>C
NM_005902.4:c.437T>C MANE Select	NP_005893.1:p.Ile146Thr
NM_001145102.2:c.122T>C	NP_001138574.1:p.Ile41Thr
NM_001145103.2:c.305T>C	NP_001138575.1:p.Ile102Thr