Canonical Allele Identifier: CA152128532

Gene: THBS2 THBS2-AS1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.*191T>G (THBS2) MANE Select	ENSP00000482784.1:n.*191T>G
ENST00000649844.1:c.*191T>G (THBS2)	ENSP00000497834.1:n.*191T>G
ENST00000676498.1:c.*191T>G (THBS2)	ENSP00000504820.1:n.*191T>G
ENST00000676628.1:c.*191T>G (THBS2)	ENSP00000504416.1:n.*191T>G
ENST00000676760.1:c.*191T>G (THBS2)	ENSP00000503020.1:n.*191T>G
ENST00000676869.1:c.*191T>G (THBS2)	ENSP00000504488.1:n.*191T>G
ENST00000676941.1:c.2829T>G (THBS2)	ENSP00000503028.1:n.2829T>G
ENST00000677429.1:c.*3076T>G (THBS2)	ENSP00000503286.1:n.*3076T>G
ENST00000678378.1:n.3095T>G (THBS2)
ENST00000366787.7:c.*191T>G (THBS2)	ENSP00000355751.3:n.*191T>G
ENST00000488355.1:n.704-6T>G (THBS2)
ENST00000617924.4:c.*191T>G (THBS2)	ENSP00000482784.1:n.*191T>G
NM_003247.3:c.*191T>G (THBS2)	NP_003238.2:n.*191T>G
XR_943307.1:n.681+3144A>C (THBS2-AS1)
NR_134621.1:n.681+3144A>C (THBS2-AS1)
NM_003247.4:c.*191T>G (THBS2)	NP_003238.2:n.*191T>G
NM_001381939.1:c.*191T>G (THBS2)	NP_001368868.1:n.*191T>G
NM_001381942.1:c.*191T>G (THBS2)	NP_001368871.1:n.*191T>G
NM_003247.5:c.*191T>G (THBS2) MANE Select	NP_003238.2:n.*191T>G
NR_167744.1:n.3865T>G (THBS2)
NR_167745.1:n.3984T>G (THBS2)