Canonical Allele Identifier: CA405998367

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41838074G>T (hg19) ; chr19:g.41332169G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332169G>T , CM000681.2:g.41332169G>T	GRCh38
NC_000019.9:g.41838074G>T , CM000681.1:g.41838074G>T	GRCh37
NC_000019.8:g.46529914G>T	NCBI36
NG_013364.1:g.26758C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.973C>A MANE Select	ENSP00000221930.4:p.Pro325Thr
ENST00000600196.2:c.825C>A	ENSP00000504008.1:p.Gly275=
ENST00000677934.1:c.747C>A	ENSP00000504769.1:p.Gly249=
ENST00000221930.5:c.973C>A	ENSP00000221930.4:p.Pro325Thr
ENST00000598758.5:c.261C>A
ENST00000600196.1:n.285C>A
NM_000660.5:c.973C>A	NP_000651.3:p.Pro325Thr
XM_011527242.1:c.976C>A	XP_011525544.1:p.Pro326Thr
NM_000660.6:c.973C>A	NP_000651.3:p.Pro325Thr
XM_011527242.2:c.976C>A	XP_011525544.1:p.Pro326Thr
NM_000660.7:c.973C>A MANE Select	NP_000651.3:p.Pro325Thr