Canonical Allele Identifier: CA8956233

Gene: SMAD2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.47868429G>A , CM000680.2:g.47868429G>A	GRCh38
NC_000018.9:g.45394800G>A , CM000680.1:g.45394800G>A	GRCh37
NC_000018.8:g.43648798G>A	NCBI36
NG_029946.1:g.67716C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005901.6:c.549C>T MANE Select	NP_005892.1:p.His183=
ENST00000262160.11:c.549C>T MANE Select	ENSP00000262160.6:p.His183=
NM_001003652.3:c.549C>T	NP_001003652.1:p.His183=
NM_001003652.4:c.549C>T	NP_001003652.1:p.His183=
NM_001135937.2:c.459C>T	NP_001129409.1:p.His153=
NM_001135937.3:c.459C>T	NP_001129409.1:p.His153=
NM_005901.5:c.549C>T	NP_005892.1:p.His183=
ENST00000262160.10:c.549C>T	ENSP00000262160.6:p.His183=
ENST00000356825.8:c.459C>T	ENSP00000349282.4:p.His153=
ENST00000402690.6:c.549C>T	ENSP00000384449.1:p.His183=
ENST00000586040.5:c.459C>T	ENSP00000466193.1:p.His153=
ENST00000586514.5:c.549C>T	ENSP00000465355.1:p.His183=
ENST00000587269.5:c.549C>T	ENSP00000466254.1:p.His183=
ENST00000587353.5:n.418C>T
ENST00000591214.5:c.459C>T	ENSP00000467075.1:p.His153=
XM_005258259.2:c.549C>T	XP_005258316.1:p.His183=
XM_005258259.4:c.549C>T	XP_005258316.1:p.His183=
XM_006722451.2:c.549C>T	XP_006722514.1:p.His183=
XM_006722451.4:c.549C>T	XP_006722514.1:p.His183=
XM_011525983.1:c.459C>T	XP_011524285.1:p.His153=
XM_011525984.1:c.423C>T	XP_011524286.1:p.His141=
XM_011525984.2:c.423C>T	XP_011524286.1:p.His141=
XM_011525985.1:c.390C>T	XP_011524287.1:p.His130=
XM_011525985.3:c.390C>T	XP_011524287.1:p.His130=
XM_017025745.2:c.549C>T	XP_016881234.1:p.His183=
XM_017025746.2:c.459C>T	XP_016881235.1:p.His153=
XM_017025747.2:c.402C>T	XP_016881236.1:p.His134=
XM_017025748.2:c.390C>T	XP_016881237.1:p.His130=
XM_017025749.1:c.549C>T	XP_016881238.1:p.His183=
XM_017025750.2:c.-218C>T	XP_016881239.1:n.-218C>T
XM_024451173.1:c.549C>T	XP_024306941.1:p.His183=