Canonical Allele Identifier: CA2627736702
Gene: THBS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39581159A>G , CM000677.2:g.39581159A>G GRCh38
NC_000015.9:g.39873360A>G , CM000677.1:g.39873360A>G GRCh37
NC_000015.8:g.37660652A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260356.6:c.-99A>G MANE Select ENSP00000260356.5:n.-99A>G
ENST00000260356.5:c.-99A>G ENSP00000260356.5:n.-99A>G
ENST00000397591.2:c.-220A>G ENSP00000380720.2:n.-220A>G
NM_003246.2:c.-99A>G NP_003237.2:n.-99A>G
NM_003246.3:c.-99A>G NP_003237.2:n.-99A>G
XM_011521970.1:c.-220A>G XP_011520272.1:n.-220A>G
XM_011521971.1:c.-99A>G XP_011520273.1:n.-99A>G
XR_931897.1:n.77A>G
XM_011521971.2:c.-99A>G XP_011520273.1:n.-99A>G
NM_003246.4:c.-99A>G MANE Select NP_003237.2:n.-99A>G