Canonical Allele Identifier: CA366460013

Gene: THBS2 THBS2-AS1

Linked Data

• MyVariant Identifiers: chr6:g.169629701T>A (hg19) ; chr6:g.169229606T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169229606T>A , CM000668.2:g.169229606T>A	GRCh38
NC_000006.11:g.169629701T>A , CM000668.1:g.169629701T>A	GRCh37
NC_000006.10:g.169371626T>A	NCBI36
NG_022911.1:g.29437A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.2225A>T (THBS2) MANE Select	ENSP00000482784.1:p.Asp742Val
ENST00000649844.1:c.2240A>T (THBS2)	ENSP00000497834.1:p.Asp747Val
ENST00000676498.1:c.2225A>T (THBS2)	ENSP00000504820.1:p.Asp742Val
ENST00000676628.1:c.2051A>T (THBS2)	ENSP00000504416.1:p.Asp684Val
ENST00000676760.1:c.2225A>T (THBS2)	ENSP00000503020.1:p.Asp742Val
ENST00000676869.1:c.2054A>T (THBS2)	ENSP00000504488.1:p.Asp685Val
ENST00000676941.1:c.1334A>T (THBS2)	ENSP00000503028.1:p.Asp445Val
ENST00000677429.1:c.*1591A>T (THBS2)	ENSP00000503286.1:n.*1591A>T
ENST00000678378.1:n.1610A>T (THBS2)
ENST00000366787.7:c.2225A>T (THBS2)	ENSP00000355751.3:p.Asp742Val
ENST00000617924.4:c.2225A>T (THBS2)	ENSP00000482784.1:p.Asp742Val
NM_003247.3:c.2225A>T (THBS2)	NP_003238.2:p.Asp742Val
XR_943307.1:n.682-9619T>A (THBS2-AS1)
NR_134621.1:n.682-9619T>A (THBS2-AS1)
NM_003247.4:c.2225A>T (THBS2)	NP_003238.2:p.Asp742Val
NM_001381939.1:c.2051A>T (THBS2)	NP_001368868.1:p.Asp684Val
NM_001381942.1:c.1994A>T (THBS2)	NP_001368871.1:p.Asp665Val
NM_003247.5:c.2225A>T (THBS2) MANE Select	NP_003238.2:p.Asp742Val
NR_167744.1:n.2370A>T (THBS2)
NR_167745.1:n.2499A>T (THBS2)