Canonical Allele Identifier: CA2184368651
Gene: SMAD3 HGNC NCBI

Linked Data

dbSNP Id: rs1959904031

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066000_67066012dup , CM000677.2:g.67066000_67066012dup GRCh38
NC_000015.9:g.67358338_67358350dup , CM000677.1:g.67358338_67358350dup GRCh37
NC_000015.8:g.65145392_65145404dup NCBI36
NG_011990.1:g.5144_5156dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2056_-110+2068dup ENSP00000453082.2:n.-110+2056_-110+2068dup
ENST00000560424.2:c.-155_-143dup ENSP00000455540.2:n.-155_-143dup
ENST00000327367.9:c.-155_-143dup MANE Select ENSP00000332973.4:n.-155_-143dup
ENST00000327367.8:c.-155_-143dup ENSP00000332973.4:n.-155_-143dup
ENST00000559460.5:c.-110+2056_-110+2068dup ENSP00000453082.1:n.-110+2056_-110+2068dup
NM_005902.3:c.-155_-143dup NP_005893.1:n.-155_-143dup
XM_011521559.1:c.-155_-143dup XP_011519861.1:n.-155_-143dup
NM_005902.4:c.-155_-143dup MANE Select NP_005893.1:n.-155_-143dup