Canonical Allele Identifier: CA2184368580
Gene: SMAD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67065944G= , CM000677.2:g.67065944G= GRCh38
NC_000015.9:g.67358282G= , CM000677.1:g.67358282G= GRCh37
NC_000015.8:g.65145336G= NCBI36
NG_011990.1:g.5088G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2000G= ENSP00000453082.2:n.-110+2000G=
ENST00000560424.2:c.-211G= ENSP00000455540.2:n.-211G=
ENST00000327367.9:c.-211G= MANE Select ENSP00000332973.4:n.-211G=
ENST00000327367.8:c.-211G= ENSP00000332973.4:n.-211G=
ENST00000559460.5:c.-110+2000G= ENSP00000453082.1:n.-110+2000G=
NM_005902.3:c.-211G= NP_005893.1:n.-211G=
XM_011521559.1:c.-211G= XP_011519861.1:n.-211G=
NM_005902.4:c.-211G= MANE Select NP_005893.1:n.-211G=
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