Canonical Allele Identifier: CA2171396526
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581200T= , CM000677.2:g.39581200T= GRCh38
NC_000015.9:g.39873401T= , CM000677.1:g.39873401T= GRCh37
NC_000015.8:g.37660693T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-58T= MANE Select ENSP00000260356.5:n.-58T=
ENST00000260356.5:c.-58T= ENSP00000260356.5:n.-58T=
ENST00000397591.2:c.-179T= ENSP00000380720.2:n.-179T=
NM_003246.2:c.-58T= NP_003237.2:n.-58T=
NM_003246.3:c.-58T= NP_003237.2:n.-58T=
XM_011521970.1:c.-179T= XP_011520272.1:n.-179T=
XM_011521971.1:c.-58T= XP_011520273.1:n.-58T=
XR_931897.1:n.118T=
XM_011521971.2:c.-58T= XP_011520273.1:n.-58T=
NM_003246.4:c.-58T= MANE Select NP_003237.2:n.-58T=