Canonical Allele Identifier: CA2171396494
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581133G= , CM000677.2:g.39581133G= GRCh38
NC_000015.9:g.39873334G= , CM000677.1:g.39873334G= GRCh37
NC_000015.8:g.37660626G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-125G= MANE Select ENSP00000260356.5:n.-125G=
ENST00000260356.5:c.-125G= ENSP00000260356.5:n.-125G=
ENST00000397591.2:c.-246G= ENSP00000380720.2:n.-246G=
NM_003246.2:c.-125G= NP_003237.2:n.-125G=
NM_003246.3:c.-125G= NP_003237.2:n.-125G=
XM_011521970.1:c.-246G= XP_011520272.1:n.-246G=
XM_011521971.1:c.-125G= XP_011520273.1:n.-125G=
XR_931897.1:n.51G=
XM_011521971.2:c.-125G= XP_011520273.1:n.-125G=
NM_003246.4:c.-125G= MANE Select NP_003237.2:n.-125G=