Canonical Allele Identifier: CA453159732
Gene: THBS2 HGNC NCBI
THBS2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.169629727C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.169229632C>T , CM000668.2:g.169229632C>T GRCh38
NC_000006.11:g.169629727C>T , CM000668.1:g.169629727C>T GRCh37
NC_000006.10:g.169371652C>T NCBI36
NG_022911.1:g.29411G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617924.6:c.2199G>A (THBS2) MANE Select ENSP00000482784.1:p.Lys733=
ENST00000649844.1:c.2214G>A (THBS2) ENSP00000497834.1:p.Lys738=
ENST00000676498.1:c.2199G>A (THBS2) ENSP00000504820.1:p.Lys733=
ENST00000676628.1:c.2025G>A (THBS2) ENSP00000504416.1:p.Lys675=
ENST00000676760.1:c.2199G>A (THBS2) ENSP00000503020.1:p.Lys733=
ENST00000676869.1:c.2028G>A (THBS2) ENSP00000504488.1:p.Lys676=
ENST00000676941.1:c.1308G>A (THBS2) ENSP00000503028.1:p.Lys436=
ENST00000677429.1:c.*1565G>A (THBS2) ENSP00000503286.1:n.*1565G>A
ENST00000678378.1:n.1584G>A (THBS2)
ENST00000366787.7:c.2199G>A (THBS2) ENSP00000355751.3:p.Lys733=
ENST00000617924.4:c.2199G>A (THBS2) ENSP00000482784.1:p.Lys733=
NM_003247.3:c.2199G>A (THBS2) NP_003238.2:p.Lys733=
XR_943307.1:n.682-9593C>T (THBS2-AS1)
NR_134621.1:n.682-9593C>T (THBS2-AS1)
NM_003247.4:c.2199G>A (THBS2) NP_003238.2:p.Lys733=
NM_001381939.1:c.2025G>A (THBS2) NP_001368868.1:p.Lys675=
NM_001381942.1:c.1968G>A (THBS2) NP_001368871.1:p.Lys656=
NM_003247.5:c.2199G>A (THBS2) MANE Select NP_003238.2:p.Lys733=
NR_167744.1:n.2344G>A (THBS2)
NR_167745.1:n.2473G>A (THBS2)