Canonical Allele Identifier: CA2184369416
Gene: SMAD3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066370C= , CM000677.2:g.67066370C= GRCh38
NC_000015.9:g.67358708C= , CM000677.1:g.67358708C= GRCh37
NC_000015.8:g.65145762C= NCBI36
NG_011990.1:g.5514C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2426C= ENSP00000453082.2:n.-110+2426C=
ENST00000560424.2:c.206+10C= ENSP00000455540.2:n.206+10C=
ENST00000327367.9:c.206+10C= MANE Select ENSP00000332973.4:n.206+10C=
ENST00000327367.8:c.206+10C= ENSP00000332973.4:n.206+10C=
ENST00000559460.5:c.-110+2426C= ENSP00000453082.1:n.-110+2426C=
NM_005902.3:c.206+10C= NP_005893.1:n.206+10C=
XM_011521559.1:c.206+10C= XP_011519861.1:n.206+10C=
XM_011521559.3:c.206+10C= XP_011519861.1:n.206+10C=
NM_005902.4:c.206+10C= MANE Select NP_005893.1:n.206+10C=
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