Canonical Allele Identifier: CA2336418814

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41337592T= , CM000681.2:g.41337592T=	GRCh38
NC_000019.9:g.41843497T= , CM000681.1:g.41843497T=	GRCh37
NC_000019.8:g.46535337T=	NCBI36
NG_013364.1:g.21335A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.860+4291A= MANE Select	ENSP00000221930.4:n.860+4291A=
ENST00000600196.2:c.712+4578A=	ENSP00000504008.1:n.712+4578A=
ENST00000677934.1:c.635-5311A=	ENSP00000504769.1:n.635-5311A=
ENST00000221930.5:c.860+4291A=	ENSP00000221930.4:n.860+4291A=
ENST00000598758.5:c.148+4291A=
ENST00000600196.1:n.172+4578A=
NM_000660.5:c.860+4291A=	NP_000651.3:n.860+4291A=
XM_011527242.1:c.863+4291A=	XP_011525544.1:n.863+4291A=
NM_000660.6:c.860+4291A=	NP_000651.3:n.860+4291A=
XM_011527242.2:c.863+4291A=	XP_011525544.1:n.863+4291A=
NM_000660.7:c.860+4291A= MANE Select	NP_000651.3:n.860+4291A=