Canonical Allele Identifier: CA2171396455
Gene: THBS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581087C= , CM000677.2:g.39581087C= GRCh38
NC_000015.9:g.39873288C= , CM000677.1:g.39873288C= GRCh37
NC_000015.8:g.37660580C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-171C= MANE Select ENSP00000260356.5:n.-171C=
ENST00000397591.2:c.-292C= ENSP00000380720.2:n.-292C=
NM_003246.2:c.-171C= NP_003237.2:n.-171C=
NM_003246.3:c.-171C= NP_003237.2:n.-171C=
XM_011521970.1:c.-292C= XP_011520272.1:n.-292C=
XM_011521971.1:c.-171C= XP_011520273.1:n.-171C=
XR_931897.1:n.5C=
XM_011521971.2:c.-171C= XP_011520273.1:n.-171C=
NM_003246.4:c.-171C= MANE Select NP_003237.2:n.-171C=