Canonical Allele Identifier: CA1584796902
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136055676G= , CM000667.2:g.136055676G= GRCh38
NC_000005.9:g.135391365G= , CM000667.1:g.135391365G= GRCh37
NC_000005.8:g.135419264G= NCBI36
NG_012646.1:g.31782G=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.1411-4G= MANE Select ENSP00000416330.2:n.1411-4G=
ENST00000442011.6:c.1411-4G= ENSP00000416330.2:n.1411-4G=
ENST00000506699.5:n.1928-4G=
ENST00000507018.5:c.1389-4G=
ENST00000509485.5:c.326-4G=
ENST00000514242.5:n.178G=
ENST00000514554.5:c.563-4G=
NM_000358.2:c.1411-4G= NP_000349.1:n.1411-4G=
NM_000358.3:c.1411-4G= MANE Select NP_000349.1:n.1411-4G=