Canonical Allele Identifier: CA2735879237

Gene: TGFB1

Linked Data

• dbSNP Id: rs200142508

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41347991_41347999dup , CM000681.2:g.41347991_41347999dup	GRCh38
NC_000019.9:g.41853896_41853904dup , CM000681.1:g.41853896_41853904dup	GRCh37
NC_000019.8:g.46545736_46545744dup	NCBI36
NG_013364.1:g.10931_10939dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.516+299_516+307dup MANE Select	ENSP00000221930.4:n.516+299_516+307dup
ENST00000600196.2:c.516+299_516+307dup	ENSP00000504008.1:n.516+299_516+307dup
ENST00000677934.1:c.516+299_516+307dup	ENSP00000504769.1:n.516+299_516+307dup
ENST00000221930.5:c.516+299_516+307dup	ENSP00000221930.4:n.516+299_516+307dup
ENST00000597453.1:n.47+299_47+307dup
NM_000660.5:c.516+299_516+307dup	NP_000651.3:n.516+299_516+307dup
XM_011527242.1:c.516+299_516+307dup	XP_011525544.1:n.516+299_516+307dup
NM_000660.6:c.516+299_516+307dup	NP_000651.3:n.516+299_516+307dup
XM_011527242.2:c.516+299_516+307dup	XP_011525544.1:n.516+299_516+307dup
NM_000660.7:c.516+299_516+307dup MANE Select	NP_000651.3:n.516+299_516+307dup