Canonical Allele Identifier: CA2184368575
Gene: SMAD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67065942G= , CM000677.2:g.67065942G= GRCh38
NC_000015.9:g.67358280G= , CM000677.1:g.67358280G= GRCh37
NC_000015.8:g.65145334G= NCBI36
NG_011990.1:g.5086G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+1998G= ENSP00000453082.2:n.-110+1998G=
ENST00000560424.2:c.-213G= ENSP00000455540.2:n.-213G=
ENST00000327367.9:c.-213G= MANE Select ENSP00000332973.4:n.-213G=
ENST00000327367.8:c.-213G= ENSP00000332973.4:n.-213G=
ENST00000559460.5:c.-110+1998G= ENSP00000453082.1:n.-110+1998G=
NM_005902.3:c.-213G= NP_005893.1:n.-213G=
XM_011521559.1:c.-213G= XP_011519861.1:n.-213G=
NM_005902.4:c.-213G= MANE Select NP_005893.1:n.-213G=
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