Canonical Allele Identifier: CA366459938
Gene: THBS2 HGNC NCBI
THBS2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1298933054

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.169229573T>A , CM000668.2:g.169229573T>A GRCh38
NC_000006.11:g.169629668T>A , CM000668.1:g.169629668T>A GRCh37
NC_000006.10:g.169371593T>A NCBI36
NG_022911.1:g.29470A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000617924.6:c.2258A>T (THBS2) MANE Select ENSP00000482784.1:p.Lys753Met
ENST00000649844.1:c.2273A>T (THBS2) ENSP00000497834.1:p.Lys758Met
ENST00000676498.1:c.2258A>T (THBS2) ENSP00000504820.1:p.Lys753Met
ENST00000676628.1:c.2084A>T (THBS2) ENSP00000504416.1:p.Lys695Met
ENST00000676760.1:c.2258A>T (THBS2) ENSP00000503020.1:p.Lys753Met
ENST00000676869.1:c.2087A>T (THBS2) ENSP00000504488.1:p.Lys696Met
ENST00000676941.1:c.1367A>T (THBS2) ENSP00000503028.1:p.Lys456Met
ENST00000677429.1:c.*1624A>T (THBS2) ENSP00000503286.1:n.*1624A>T
ENST00000678378.1:n.1643A>T (THBS2)
ENST00000366787.7:c.2258A>T (THBS2) ENSP00000355751.3:p.Lys753Met
ENST00000617924.4:c.2258A>T (THBS2) ENSP00000482784.1:p.Lys753Met
NM_003247.3:c.2258A>T (THBS2) NP_003238.2:p.Lys753Met
XR_943307.1:n.682-9652T>A (THBS2-AS1)
NR_134621.1:n.682-9652T>A (THBS2-AS1)
NM_003247.4:c.2258A>T (THBS2) NP_003238.2:p.Lys753Met
NM_001381939.1:c.2084A>T (THBS2) NP_001368868.1:p.Lys695Met
NM_001381942.1:c.2027A>T (THBS2) NP_001368871.1:p.Lys676Met
NM_003247.5:c.2258A>T (THBS2) MANE Select NP_003238.2:p.Lys753Met
NR_167744.1:n.2403A>T (THBS2)
NR_167745.1:n.2532A>T (THBS2)