Canonical Allele Identifier: CA308510980

Gene: TGFB1

Linked Data

• dbSNP Id: rs755586793
• MyVariant Identifiers: chr19:g.41848353_41848391del (hg19) ; chr19:g.41342448_41342486del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342449_41342487del , CM000681.2:g.41342449_41342487del	GRCh38
NC_000019.9:g.41848354_41848392del , CM000681.1:g.41848354_41848392del	GRCh37
NC_000019.8:g.46540194_46540232del	NCBI36
NG_013364.1:g.16441_16479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-239_635-201del MANE Select	ENSP00000221930.4:n.635-239_635-201del
ENST00000600196.2:c.635-239_635-201del	ENSP00000504008.1:n.635-239_635-201del
ENST00000677934.1:c.634+2261_634+2299del	ENSP00000504769.1:n.634+2261_634+2299del
ENST00000221930.5:c.635-239_635-201del	ENSP00000221930.4:n.635-239_635-201del
ENST00000597453.1:n.166-239_166-201del
ENST00000600196.1:n.95-239_95-201del
NM_000660.5:c.635-239_635-201del	NP_000651.3:n.635-239_635-201del
XM_011527242.1:c.635-239_635-201del	XP_011525544.1:n.635-239_635-201del
NM_000660.6:c.635-239_635-201del	NP_000651.3:n.635-239_635-201del
XM_011527242.2:c.635-239_635-201del	XP_011525544.1:n.635-239_635-201del
NM_000660.7:c.635-239_635-201del MANE Select	NP_000651.3:n.635-239_635-201del