Canonical Allele Identifier: CA882316879

Gene: TGFB1

Linked Data

• dbSNP Id: rs1491272425
• MyVariant Identifiers: chr19:g.41848318_41848319insG (hg19) ; chr19:g.41342413_41342414insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342414dup , CM000681.2:g.41342414dup	GRCh38
NC_000019.9:g.41848319dup , CM000681.1:g.41848319dup	GRCh37
NC_000019.8:g.46540159dup	NCBI36
NG_013364.1:g.16513dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-167dup MANE Select	ENSP00000221930.4:n.635-167dup
ENST00000600196.2:c.635-167dup	ENSP00000504008.1:n.635-167dup
ENST00000677934.1:c.634+2333dup	ENSP00000504769.1:n.634+2333dup
ENST00000221930.5:c.635-167dup	ENSP00000221930.4:n.635-167dup
ENST00000597453.1:n.166-167dup
ENST00000600196.1:n.95-167dup
NM_000660.5:c.635-167dup	NP_000651.3:n.635-167dup
XM_011527242.1:c.635-167dup	XP_011525544.1:n.635-167dup
NM_000660.6:c.635-167dup	NP_000651.3:n.635-167dup
XM_011527242.2:c.635-167dup	XP_011525544.1:n.635-167dup
NM_000660.7:c.635-167dup MANE Select	NP_000651.3:n.635-167dup