Canonical Allele Identifier: CA268716651

Gene: THBS1

Linked Data

• dbSNP Id: rs953468454
• MyVariant Identifiers: chr15:g.39873456G>A (hg19) ; chr15:g.39581255G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.39581255G>A , CM000677.2:g.39581255G>A	GRCh38
NC_000015.9:g.39873456G>A , CM000677.1:g.39873456G>A	GRCh37
NC_000015.8:g.37660748G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260356.6:c.-30+27G>A MANE Select	ENSP00000260356.5:n.-30+27G>A
ENST00000260356.5:c.-30+27G>A	ENSP00000260356.5:n.-30+27G>A
ENST00000397591.2:c.-151+27G>A	ENSP00000380720.2:n.-151+27G>A
NM_003246.2:c.-30+27G>A	NP_003237.2:n.-30+27G>A
NM_003246.3:c.-30+27G>A	NP_003237.2:n.-30+27G>A
XM_011521970.1:c.-151+27G>A	XP_011520272.1:n.-151+27G>A
XM_011521971.1:c.-30+27G>A	XP_011520273.1:n.-30+27G>A
XR_931897.1:n.146+27G>A
XM_011521971.2:c.-30+27G>A	XP_011520273.1:n.-30+27G>A
NM_003246.4:c.-30+27G>A MANE Select	NP_003237.2:n.-30+27G>A