Canonical Allele Identifier: CA2171396515
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581177G= , CM000677.2:g.39581177G= GRCh38
NC_000015.9:g.39873378G= , CM000677.1:g.39873378G= GRCh37
NC_000015.8:g.37660670G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-81G= MANE Select ENSP00000260356.5:n.-81G=
ENST00000260356.5:c.-81G= ENSP00000260356.5:n.-81G=
ENST00000397591.2:c.-202G= ENSP00000380720.2:n.-202G=
NM_003246.2:c.-81G= NP_003237.2:n.-81G=
NM_003246.3:c.-81G= NP_003237.2:n.-81G=
XM_011521970.1:c.-202G= XP_011520272.1:n.-202G=
XM_011521971.1:c.-81G= XP_011520273.1:n.-81G=
XR_931897.1:n.95G=
XM_011521971.2:c.-81G= XP_011520273.1:n.-81G=
NM_003246.4:c.-81G= MANE Select NP_003237.2:n.-81G=