Canonical Allele Identifier: CA405998733

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41838178T>A (hg19) ; chr19:g.41332273T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332273T>A , CM000681.2:g.41332273T>A	GRCh38
NC_000019.9:g.41838178T>A , CM000681.1:g.41838178T>A	GRCh37
NC_000019.8:g.46530018T>A	NCBI36
NG_013364.1:g.26654A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.869A>T MANE Select	ENSP00000221930.4:p.Glu290Val
ENST00000600196.2:c.721A>T	ENSP00000504008.1:p.Arg241Ter
ENST00000677934.1:c.643A>T	ENSP00000504769.1:p.Arg215Ter
ENST00000221930.5:c.869A>T	ENSP00000221930.4:p.Glu290Val
ENST00000598758.5:c.157A>T
ENST00000600196.1:n.181A>T
NM_000660.5:c.869A>T	NP_000651.3:p.Glu290Val
XM_011527242.1:c.872A>T	XP_011525544.1:p.Glu291Val
NM_000660.6:c.869A>T	NP_000651.3:p.Glu290Val
XM_011527242.2:c.872A>T	XP_011525544.1:p.Glu291Val
NM_000660.7:c.869A>T MANE Select	NP_000651.3:p.Glu290Val