Canonical Allele Identifier: CA882316922

Gene: TGFB1

Linked Data

• dbSNP Id: rs1468231833
• MyVariant Identifiers: chr19:g.41848376_41848377insCCCGA (hg19) ; chr19:g.41342471_41342472insCCCGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342472_41342476dup , CM000681.2:g.41342472_41342476dup	GRCh38
NC_000019.9:g.41848377_41848381dup , CM000681.1:g.41848377_41848381dup	GRCh37
NC_000019.8:g.46540217_46540221dup	NCBI36
NG_013364.1:g.16451_16455dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-229_635-225dup MANE Select	ENSP00000221930.4:n.635-229_635-225dup
ENST00000600196.2:c.635-229_635-225dup	ENSP00000504008.1:n.635-229_635-225dup
ENST00000677934.1:c.634+2271_634+2275dup	ENSP00000504769.1:n.634+2271_634+2275dup
ENST00000221930.5:c.635-229_635-225dup	ENSP00000221930.4:n.635-229_635-225dup
ENST00000597453.1:n.166-229_166-225dup
ENST00000600196.1:n.95-229_95-225dup
NM_000660.5:c.635-229_635-225dup	NP_000651.3:n.635-229_635-225dup
XM_011527242.1:c.635-229_635-225dup	XP_011525544.1:n.635-229_635-225dup
NM_000660.6:c.635-229_635-225dup	NP_000651.3:n.635-229_635-225dup
XM_011527242.2:c.635-229_635-225dup	XP_011525544.1:n.635-229_635-225dup
NM_000660.7:c.635-229_635-225dup MANE Select	NP_000651.3:n.635-229_635-225dup