Canonical Allele Identifier: CA2336421080

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342123C= , CM000681.2:g.41342123C=	GRCh38
NC_000019.9:g.41848028C= , CM000681.1:g.41848028C=	GRCh37
NC_000019.8:g.46539868C=	NCBI36
NG_013364.1:g.16804G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.712+47G= MANE Select	ENSP00000221930.4:n.712+47G=
ENST00000600196.2:c.712+47G=	ENSP00000504008.1:n.712+47G=
ENST00000677934.1:c.634+2624G=	ENSP00000504769.1:n.634+2624G=
ENST00000221930.5:c.712+47G=	ENSP00000221930.4:n.712+47G=
ENST00000597453.1:n.290G=
ENST00000600196.1:n.172+47G=
NM_000660.5:c.712+47G=	NP_000651.3:n.712+47G=
XM_011527242.1:c.712+47G=	XP_011525544.1:n.712+47G=
NM_000660.6:c.712+47G=	NP_000651.3:n.712+47G=
XM_011527242.2:c.712+47G=	XP_011525544.1:n.712+47G=
NM_000660.7:c.712+47G= MANE Select	NP_000651.3:n.712+47G=