Canonical Allele Identifier: CA618686772

Gene: SMAD3

Linked Data

• dbSNP Id: rs1343206731
• gnomAD v2: 15-67458523-G-A
• gnomAD v4: 15-67166185-G-A
• MyVariant Identifiers: chr15:g.67458523G>A (hg19) ; chr15:g.67166185G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67166185G>A , CM000677.2:g.67166185G>A	GRCh38
NC_000015.9:g.67458523G>A , CM000677.1:g.67458523G>A	GRCh37
NC_000015.8:g.65245577G>A	NCBI36
NG_011990.1:g.105329G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.218-594G>A	ENSP00000453684.2:n.218-594G>A
ENST00000559460.6:c.218-594G>A	ENSP00000453082.2:n.218-594G>A
ENST00000560424.2:c.533-594G>A	ENSP00000455540.2:n.533-594G>A
ENST00000327367.9:c.533-594G>A MANE Select	ENSP00000332973.4:n.533-594G>A
ENST00000679624.1:c.218-594G>A	ENSP00000505445.1:n.218-594G>A
ENST00000681239.1:c.218-594G>A	ENSP00000505641.1:n.218-594G>A
ENST00000327367.8:c.533-594G>A	ENSP00000332973.4:n.533-594G>A
ENST00000439724.7:c.401-594G>A	ENSP00000401133.3:n.401-594G>A
ENST00000537194.6:c.-62G>A	ENSP00000445348.2:n.-62G>A
ENST00000540846.6:c.218-594G>A	ENSP00000437757.2:n.218-594G>A
ENST00000558894.5:c.218-594G>A	ENSP00000458060.1:n.218-594G>A
ENST00000559460.5:c.218-594G>A	ENSP00000453082.1:n.218-594G>A
ENST00000559937.1:n.383-594G>A
ENST00000560175.5:c.218-594G>A	ENSP00000455095.1:n.218-594G>A
NM_001145102.1:c.218-594G>A	NP_001138574.1:n.218-594G>A
NM_001145103.1:c.401-594G>A	NP_001138575.1:n.401-594G>A
NM_001145104.1:c.-62G>A	NP_001138576.1:n.-62G>A
NM_005902.3:c.533-594G>A	NP_005893.1:n.533-594G>A
XM_011521559.1:c.401-594G>A	XP_011519861.1:n.401-594G>A
XM_011521560.1:c.386-594G>A	XP_011519862.1:n.386-594G>A
XM_011521559.3:c.401-594G>A	XP_011519861.1:n.401-594G>A
NM_005902.4:c.533-594G>A MANE Select	NP_005893.1:n.533-594G>A
NM_001145102.2:c.218-594G>A	NP_001138574.1:n.218-594G>A
NM_001145103.2:c.401-594G>A	NP_001138575.1:n.401-594G>A
NM_001145104.2:c.-62G>A	NP_001138576.1:n.-62G>A