Canonical Allele Identifier: CA10646489
Gene: SMAD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 316852
dbSNP Id: rs886051373

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67065890T>G , CM000677.2:g.67065890T>G GRCh38
NC_000015.9:g.67358228T>G , CM000677.1:g.67358228T>G GRCh37
NC_000015.8:g.65145282T>G NCBI36
NG_011990.1:g.5034T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559460.6:c.-110+1946T>G ENSP00000453082.2:n.-110+1946T>G
ENST00000560424.2:c.-265T>G ENSP00000455540.2:n.-265T>G
ENST00000327367.9:c.-265T>G MANE Select ENSP00000332973.4:n.-265T>G
ENST00000327367.8:c.-265T>G ENSP00000332973.4:n.-265T>G
ENST00000559460.5:c.-110+1946T>G ENSP00000453082.1:n.-110+1946T>G
NM_005902.3:c.-265T>G NP_005893.1:n.-265T>G
XM_011521559.1:c.-265T>G XP_011519861.1:n.-265T>G
NM_005902.4:c.-265T>G MANE Select NP_005893.1:n.-265T>G