Canonical Allele Identifier: CA2171396521
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581190T= , CM000677.2:g.39581190T= GRCh38
NC_000015.9:g.39873391T= , CM000677.1:g.39873391T= GRCh37
NC_000015.8:g.37660683T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-68T= MANE Select ENSP00000260356.5:n.-68T=
ENST00000260356.5:c.-68T= ENSP00000260356.5:n.-68T=
ENST00000397591.2:c.-189T= ENSP00000380720.2:n.-189T=
NM_003246.2:c.-68T= NP_003237.2:n.-68T=
NM_003246.3:c.-68T= NP_003237.2:n.-68T=
XM_011521970.1:c.-189T= XP_011520272.1:n.-189T=
XM_011521971.1:c.-68T= XP_011520273.1:n.-68T=
XR_931897.1:n.108T=
XM_011521971.2:c.-68T= XP_011520273.1:n.-68T=
NM_003246.4:c.-68T= MANE Select NP_003237.2:n.-68T=