Canonical Allele Identifier: CA366460160

Gene: THBS2 THBS2-AS1

Linked Data

• MyVariant Identifiers: chr6:g.169629765G>T (hg19) ; chr6:g.169229670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169229670G>T , CM000668.2:g.169229670G>T	GRCh38
NC_000006.11:g.169629765G>T , CM000668.1:g.169629765G>T	GRCh37
NC_000006.10:g.169371690G>T	NCBI36
NG_022911.1:g.29373C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.2161C>A (THBS2) MANE Select	ENSP00000482784.1:p.Pro721Thr
ENST00000649844.1:c.2176C>A (THBS2)	ENSP00000497834.1:p.Pro726Thr
ENST00000676498.1:c.2161C>A (THBS2)	ENSP00000504820.1:p.Pro721Thr
ENST00000676628.1:c.1987C>A (THBS2)	ENSP00000504416.1:p.Pro663Thr
ENST00000676760.1:c.2161C>A (THBS2)	ENSP00000503020.1:p.Pro721Thr
ENST00000676869.1:c.1990C>A (THBS2)	ENSP00000504488.1:p.Pro664Thr
ENST00000676941.1:c.1270C>A (THBS2)	ENSP00000503028.1:p.Pro424Thr
ENST00000677429.1:c.*1527C>A (THBS2)	ENSP00000503286.1:n.*1527C>A
ENST00000678378.1:n.1546C>A (THBS2)
ENST00000366787.7:c.2161C>A (THBS2)	ENSP00000355751.3:p.Pro721Thr
ENST00000617924.4:c.2161C>A (THBS2)	ENSP00000482784.1:p.Pro721Thr
NM_003247.3:c.2161C>A (THBS2)	NP_003238.2:p.Pro721Thr
XR_943307.1:n.682-9555G>T (THBS2-AS1)
NR_134621.1:n.682-9555G>T (THBS2-AS1)
NM_003247.4:c.2161C>A (THBS2)	NP_003238.2:p.Pro721Thr
NM_001381939.1:c.1987C>A (THBS2)	NP_001368868.1:p.Pro663Thr
NM_001381942.1:c.1930C>A (THBS2)	NP_001368871.1:p.Pro644Thr
NM_003247.5:c.2161C>A (THBS2) MANE Select	NP_003238.2:p.Pro721Thr
NR_167744.1:n.2306C>A (THBS2)
NR_167745.1:n.2435C>A (THBS2)