Canonical Allele Identifier: CA393202767
Gene: SMAD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.67358544T>A (hg19) chr15:g.67066206T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066206T>A , CM000677.2:g.67066206T>A GRCh38
NC_000015.9:g.67358544T>A , CM000677.1:g.67358544T>A GRCh37
NC_000015.8:g.65145598T>A NCBI36
NG_011990.1:g.5350T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2262T>A ENSP00000453082.2:n.-110+2262T>A
ENST00000560424.2:c.52T>A ENSP00000455540.2:p.Trp18Arg
ENST00000327367.9:c.52T>A MANE Select ENSP00000332973.4:p.Trp18Arg
ENST00000327367.8:c.52T>A ENSP00000332973.4:p.Trp18Arg
ENST00000559460.5:c.-110+2262T>A ENSP00000453082.1:n.-110+2262T>A
NM_005902.3:c.52T>A NP_005893.1:p.Trp18Arg
XM_011521559.1:c.52T>A XP_011519861.1:p.Trp18Arg
XM_011521559.3:c.52T>A XP_011519861.1:p.Trp18Arg
NM_005902.4:c.52T>A MANE Select NP_005893.1:p.Trp18Arg
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