Canonical Allele Identifier: CA453159737

Gene: THBS2 THBS2-AS1

Linked Data

• MyVariant Identifiers: chr6:g.169629742C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169229647C>T , CM000668.2:g.169229647C>T	GRCh38
NC_000006.11:g.169629742C>T , CM000668.1:g.169629742C>T	GRCh37
NC_000006.10:g.169371667C>T	NCBI36
NG_022911.1:g.29396G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.2184G>A (THBS2) MANE Select	ENSP00000482784.1:p.Gln728=
ENST00000649844.1:c.2199G>A (THBS2)	ENSP00000497834.1:p.Gln733=
ENST00000676498.1:c.2184G>A (THBS2)	ENSP00000504820.1:p.Gln728=
ENST00000676628.1:c.2010G>A (THBS2)	ENSP00000504416.1:p.Gln670=
ENST00000676760.1:c.2184G>A (THBS2)	ENSP00000503020.1:p.Gln728=
ENST00000676869.1:c.2013G>A (THBS2)	ENSP00000504488.1:p.Gln671=
ENST00000676941.1:c.1293G>A (THBS2)	ENSP00000503028.1:p.Gln431=
ENST00000677429.1:c.*1550G>A (THBS2)	ENSP00000503286.1:n.*1550G>A
ENST00000678378.1:n.1569G>A (THBS2)
ENST00000366787.7:c.2184G>A (THBS2)	ENSP00000355751.3:p.Gln728=
ENST00000617924.4:c.2184G>A (THBS2)	ENSP00000482784.1:p.Gln728=
NM_003247.3:c.2184G>A (THBS2)	NP_003238.2:p.Gln728=
XR_943307.1:n.682-9578C>T (THBS2-AS1)
NR_134621.1:n.682-9578C>T (THBS2-AS1)
NM_003247.4:c.2184G>A (THBS2)	NP_003238.2:p.Gln728=
NM_001381939.1:c.2010G>A (THBS2)	NP_001368868.1:p.Gln670=
NM_001381942.1:c.1953G>A (THBS2)	NP_001368871.1:p.Gln651=
NM_003247.5:c.2184G>A (THBS2) MANE Select	NP_003238.2:p.Gln728=
NR_167744.1:n.2329G>A (THBS2)
NR_167745.1:n.2458G>A (THBS2)