Canonical Allele Identifier: CA393202741
Gene: SMAD3 HGNC NCBI

Linked Data

dbSNP Id: rs1959911549
MyVariant Identifiers: chr15:g.67358530A>C (hg19) chr15:g.67066192A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67066192A>C , CM000677.2:g.67066192A>C GRCh38
NC_000015.9:g.67358530A>C , CM000677.1:g.67358530A>C GRCh37
NC_000015.8:g.65145584A>C NCBI36
NG_011990.1:g.5336A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559460.6:c.-110+2248A>C ENSP00000453082.2:n.-110+2248A>C
ENST00000560424.2:c.38A>C ENSP00000455540.2:p.Lys13Thr
ENST00000327367.9:c.38A>C MANE Select ENSP00000332973.4:p.Lys13Thr
ENST00000327367.8:c.38A>C ENSP00000332973.4:p.Lys13Thr
ENST00000559460.5:c.-110+2248A>C ENSP00000453082.1:n.-110+2248A>C
NM_005902.3:c.38A>C NP_005893.1:p.Lys13Thr
XM_011521559.1:c.38A>C XP_011519861.1:p.Lys13Thr
XM_011521559.3:c.38A>C XP_011519861.1:p.Lys13Thr
NM_005902.4:c.38A>C MANE Select NP_005893.1:p.Lys13Thr
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