Canonical Allele Identifier: CA366460022

Gene: THBS2 THBS2-AS1

Linked Data

• MyVariant Identifiers: chr6:g.169629704T>C (hg19) ; chr6:g.169229609T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169229609T>C , CM000668.2:g.169229609T>C	GRCh38
NC_000006.11:g.169629704T>C , CM000668.1:g.169629704T>C	GRCh37
NC_000006.10:g.169371629T>C	NCBI36
NG_022911.1:g.29434A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.2222A>G (THBS2) MANE Select	ENSP00000482784.1:p.Asp741Gly
ENST00000649844.1:c.2237A>G (THBS2)	ENSP00000497834.1:p.Asp746Gly
ENST00000676498.1:c.2222A>G (THBS2)	ENSP00000504820.1:p.Asp741Gly
ENST00000676628.1:c.2048A>G (THBS2)	ENSP00000504416.1:p.Asp683Gly
ENST00000676760.1:c.2222A>G (THBS2)	ENSP00000503020.1:p.Asp741Gly
ENST00000676869.1:c.2051A>G (THBS2)	ENSP00000504488.1:p.Asp684Gly
ENST00000676941.1:c.1331A>G (THBS2)	ENSP00000503028.1:p.Asp444Gly
ENST00000677429.1:c.*1588A>G (THBS2)	ENSP00000503286.1:n.*1588A>G
ENST00000678378.1:n.1607A>G (THBS2)
ENST00000366787.7:c.2222A>G (THBS2)	ENSP00000355751.3:p.Asp741Gly
ENST00000617924.4:c.2222A>G (THBS2)	ENSP00000482784.1:p.Asp741Gly
NM_003247.3:c.2222A>G (THBS2)	NP_003238.2:p.Asp741Gly
XR_943307.1:n.682-9616T>C (THBS2-AS1)
NR_134621.1:n.682-9616T>C (THBS2-AS1)
NM_003247.4:c.2222A>G (THBS2)	NP_003238.2:p.Asp741Gly
NM_001381939.1:c.2048A>G (THBS2)	NP_001368868.1:p.Asp683Gly
NM_001381942.1:c.1991A>G (THBS2)	NP_001368871.1:p.Asp664Gly
NM_003247.5:c.2222A>G (THBS2) MANE Select	NP_003238.2:p.Asp741Gly
NR_167744.1:n.2367A>G (THBS2)
NR_167745.1:n.2496A>G (THBS2)