Canonical Allele Identifier: CA2171396536
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581216C= , CM000677.2:g.39581216C= GRCh38
NC_000015.9:g.39873417C= , CM000677.1:g.39873417C= GRCh37
NC_000015.8:g.37660709C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-42C= MANE Select ENSP00000260356.5:n.-42C=
ENST00000260356.5:c.-42C= ENSP00000260356.5:n.-42C=
ENST00000397591.2:c.-163C= ENSP00000380720.2:n.-163C=
NM_003246.2:c.-42C= NP_003237.2:n.-42C=
NM_003246.3:c.-42C= NP_003237.2:n.-42C=
XM_011521970.1:c.-163C= XP_011520272.1:n.-163C=
XM_011521971.1:c.-42C= XP_011520273.1:n.-42C=
XR_931897.1:n.134C=
XM_011521971.2:c.-42C= XP_011520273.1:n.-42C=
NM_003246.4:c.-42C= MANE Select NP_003237.2:n.-42C=