Canonical Allele Identifier: CA366460132

Gene: THBS2 THBS2-AS1

Linked Data

• MyVariant Identifiers: chr6:g.169629751A>T (hg19) ; chr6:g.169229656A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169229656A>T , CM000668.2:g.169229656A>T	GRCh38
NC_000006.11:g.169629751A>T , CM000668.1:g.169629751A>T	GRCh37
NC_000006.10:g.169371676A>T	NCBI36
NG_022911.1:g.29387T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.2175T>A (THBS2) MANE Select	ENSP00000482784.1:p.Asn725Lys
ENST00000649844.1:c.2190T>A (THBS2)	ENSP00000497834.1:p.Asn730Lys
ENST00000676498.1:c.2175T>A (THBS2)	ENSP00000504820.1:p.Asn725Lys
ENST00000676628.1:c.2001T>A (THBS2)	ENSP00000504416.1:p.Asn667Lys
ENST00000676760.1:c.2175T>A (THBS2)	ENSP00000503020.1:p.Asn725Lys
ENST00000676869.1:c.2004T>A (THBS2)	ENSP00000504488.1:p.Asn668Lys
ENST00000676941.1:c.1284T>A (THBS2)	ENSP00000503028.1:p.Asn428Lys
ENST00000677429.1:c.*1541T>A (THBS2)	ENSP00000503286.1:n.*1541T>A
ENST00000678378.1:n.1560T>A (THBS2)
ENST00000366787.7:c.2175T>A (THBS2)	ENSP00000355751.3:p.Asn725Lys
ENST00000617924.4:c.2175T>A (THBS2)	ENSP00000482784.1:p.Asn725Lys
NM_003247.3:c.2175T>A (THBS2)	NP_003238.2:p.Asn725Lys
XR_943307.1:n.682-9569A>T (THBS2-AS1)
NR_134621.1:n.682-9569A>T (THBS2-AS1)
NM_003247.4:c.2175T>A (THBS2)	NP_003238.2:p.Asn725Lys
NM_001381939.1:c.2001T>A (THBS2)	NP_001368868.1:p.Asn667Lys
NM_001381942.1:c.1944T>A (THBS2)	NP_001368871.1:p.Asn648Lys
NM_003247.5:c.2175T>A (THBS2) MANE Select	NP_003238.2:p.Asn725Lys
NR_167744.1:n.2320T>A (THBS2)
NR_167745.1:n.2449T>A (THBS2)