Canonical Allele Identifier: CA2171396534
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581213G= , CM000677.2:g.39581213G= GRCh38
NC_000015.9:g.39873414G= , CM000677.1:g.39873414G= GRCh37
NC_000015.8:g.37660706G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-45G= MANE Select ENSP00000260356.5:n.-45G=
ENST00000260356.5:c.-45G= ENSP00000260356.5:n.-45G=
ENST00000397591.2:c.-166G= ENSP00000380720.2:n.-166G=
NM_003246.2:c.-45G= NP_003237.2:n.-45G=
NM_003246.3:c.-45G= NP_003237.2:n.-45G=
XM_011521970.1:c.-166G= XP_011520272.1:n.-166G=
XM_011521971.1:c.-45G= XP_011520273.1:n.-45G=
XR_931897.1:n.131G=
XM_011521971.2:c.-45G= XP_011520273.1:n.-45G=
NM_003246.4:c.-45G= MANE Select NP_003237.2:n.-45G=