Canonical Allele Identifier: CA406003618

Gene: TGFB1

Linked Data

• MyVariant Identifiers: chr19:g.41854258G>A (hg19) ; chr19:g.41348353G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348353G>A , CM000681.2:g.41348353G>A	GRCh38
NC_000019.9:g.41854258G>A , CM000681.1:g.41854258G>A	GRCh37
NC_000019.8:g.46546098G>A	NCBI36
NG_013364.1:g.10574C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.458C>T MANE Select	ENSP00000221930.4:p.Ala153Val
ENST00000600196.2:c.458C>T	ENSP00000504008.1:p.Ala153Val
ENST00000677934.1:c.458C>T	ENSP00000504769.1:p.Ala153Val
ENST00000221930.5:c.458C>T	ENSP00000221930.4:p.Ala153Val
NM_000660.5:c.458C>T	NP_000651.3:p.Ala153Val
XM_011527242.1:c.458C>T	XP_011525544.1:p.Ala153Val
NM_000660.6:c.458C>T	NP_000651.3:p.Ala153Val
XM_011527242.2:c.458C>T	XP_011525544.1:p.Ala153Val
NM_000660.7:c.458C>T MANE Select	NP_000651.3:p.Ala153Val