Canonical Allele Identifier: CA2171396554
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581244C= , CM000677.2:g.39581244C= GRCh38
NC_000015.9:g.39873445C= , CM000677.1:g.39873445C= GRCh37
NC_000015.8:g.37660737C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-30+16C= MANE Select ENSP00000260356.5:n.-30+16C=
ENST00000260356.5:c.-30+16C= ENSP00000260356.5:n.-30+16C=
ENST00000397591.2:c.-151+16C= ENSP00000380720.2:n.-151+16C=
NM_003246.2:c.-30+16C= NP_003237.2:n.-30+16C=
NM_003246.3:c.-30+16C= NP_003237.2:n.-30+16C=
XM_011521970.1:c.-151+16C= XP_011520272.1:n.-151+16C=
XM_011521971.1:c.-30+16C= XP_011520273.1:n.-30+16C=
XR_931897.1:n.146+16C=
XM_011521971.2:c.-30+16C= XP_011520273.1:n.-30+16C=
NM_003246.4:c.-30+16C= MANE Select NP_003237.2:n.-30+16C=