Canonical Allele Identifier: CA406003589

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41854241T>A (hg19) ; chr19:g.41348336T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348336T>A , CM000681.2:g.41348336T>A	GRCh38
NC_000019.9:g.41854241T>A , CM000681.1:g.41854241T>A	GRCh37
NC_000019.8:g.46546081T>A	NCBI36
NG_013364.1:g.10591A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.475A>T MANE Select	ENSP00000221930.4:p.Arg159Trp
ENST00000600196.2:c.475A>T	ENSP00000504008.1:p.Arg159Trp
ENST00000677934.1:c.475A>T	ENSP00000504769.1:p.Arg159Trp
ENST00000221930.5:c.475A>T	ENSP00000221930.4:p.Arg159Trp
ENST00000597453.1:n.6A>T
NM_000660.5:c.475A>T	NP_000651.3:p.Arg159Trp
XM_011527242.1:c.475A>T	XP_011525544.1:p.Arg159Trp
NM_000660.6:c.475A>T	NP_000651.3:p.Arg159Trp
XM_011527242.2:c.475A>T	XP_011525544.1:p.Arg159Trp
NM_000660.7:c.475A>T MANE Select	NP_000651.3:p.Arg159Trp