Canonical Allele Identifier: CA2581606493
Gene: THBS2 HGNC NCBI
THBS2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.169217631A>T , CM000668.2:g.169217631A>T GRCh38
NC_000006.11:g.169617726A>T , CM000668.1:g.169617726A>T GRCh37
NC_000006.10:g.169359651A>T NCBI36
NG_022911.1:g.41412T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617924.6:c.*191T>A (THBS2) MANE Select ENSP00000482784.1:n.*191T>A
ENST00000649844.1:c.*191T>A (THBS2) ENSP00000497834.1:n.*191T>A
ENST00000676498.1:c.*191T>A (THBS2) ENSP00000504820.1:n.*191T>A
ENST00000676628.1:c.*191T>A (THBS2) ENSP00000504416.1:n.*191T>A
ENST00000676760.1:c.*191T>A (THBS2) ENSP00000503020.1:n.*191T>A
ENST00000676869.1:c.*191T>A (THBS2) ENSP00000504488.1:n.*191T>A
ENST00000676941.1:c.2829T>A (THBS2) ENSP00000503028.1:n.2829T>A
ENST00000677429.1:c.*3076T>A (THBS2) ENSP00000503286.1:n.*3076T>A
ENST00000678378.1:n.3095T>A (THBS2)
ENST00000366787.7:c.*191T>A (THBS2) ENSP00000355751.3:n.*191T>A
ENST00000488355.1:n.704-6T>A (THBS2)
ENST00000617924.4:c.*191T>A (THBS2) ENSP00000482784.1:n.*191T>A
NM_003247.3:c.*191T>A (THBS2) NP_003238.2:n.*191T>A
XR_943307.1:n.681+3144A>T (THBS2-AS1)
NR_134621.1:n.681+3144A>T (THBS2-AS1)
NM_003247.4:c.*191T>A (THBS2) NP_003238.2:n.*191T>A
NM_001381939.1:c.*191T>A (THBS2) NP_001368868.1:n.*191T>A
NM_001381942.1:c.*191T>A (THBS2) NP_001368871.1:n.*191T>A
NM_003247.5:c.*191T>A (THBS2) MANE Select NP_003238.2:n.*191T>A
NR_167744.1:n.3865T>A (THBS2)
NR_167745.1:n.3984T>A (THBS2)
Search 100 bp 5'
Search 100 bp 3'