Canonical Allele Identifier: CA2336423863

Gene: TGFB1

Linked Data

• dbSNP Id: rs2038138276

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348142_41348143insG , CM000681.2:g.41348142_41348143insG	GRCh38
NC_000019.9:g.41854047_41854048insG , CM000681.1:g.41854047_41854048insG	GRCh37
NC_000019.8:g.46545887_46545888insG	NCBI36
NG_013364.1:g.10784_10785insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.516+152_516+153insC MANE Select	ENSP00000221930.4:n.516+152_516+153insC
ENST00000600196.2:c.516+152_516+153insC	ENSP00000504008.1:n.516+152_516+153insC
ENST00000677934.1:c.516+152_516+153insC	ENSP00000504769.1:n.516+152_516+153insC
ENST00000221930.5:c.516+152_516+153insC	ENSP00000221930.4:n.516+152_516+153insC
ENST00000597453.1:n.47+152_47+153insC
NM_000660.5:c.516+152_516+153insC	NP_000651.3:n.516+152_516+153insC
XM_011527242.1:c.516+152_516+153insC	XP_011525544.1:n.516+152_516+153insC
NM_000660.6:c.516+152_516+153insC	NP_000651.3:n.516+152_516+153insC
XM_011527242.2:c.516+152_516+153insC	XP_011525544.1:n.516+152_516+153insC
NM_000660.7:c.516+152_516+153insC MANE Select	NP_000651.3:n.516+152_516+153insC