Canonical Allele Identifier: CA2502420788
Gene: SMAD3 HGNC NCBI

Linked Data

gnomAD v4: 15-67066053-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066053A>G , CM000677.2:g.67066053A>G GRCh38
NC_000015.9:g.67358391A>G , CM000677.1:g.67358391A>G GRCh37
NC_000015.8:g.65145445A>G NCBI36
NG_011990.1:g.5197A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000559460.6:c.-110+2109A>G ENSP00000453082.2:n.-110+2109A>G
ENST00000560424.2:c.-102A>G ENSP00000455540.2:n.-102A>G
ENST00000327367.9:c.-102A>G MANE Select ENSP00000332973.4:n.-102A>G
ENST00000327367.8:c.-102A>G ENSP00000332973.4:n.-102A>G
ENST00000559460.5:c.-110+2109A>G ENSP00000453082.1:n.-110+2109A>G
NM_005902.3:c.-102A>G NP_005893.1:n.-102A>G
XM_011521559.1:c.-102A>G XP_011519861.1:n.-102A>G
NM_005902.4:c.-102A>G MANE Select NP_005893.1:n.-102A>G
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