Canonical Allele Identifier: CA1584797055
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136055736G= , CM000667.2:g.136055736G= GRCh38
NC_000005.9:g.135391425G= , CM000667.1:g.135391425G= GRCh37
NC_000005.8:g.135419324G= NCBI36
NG_012646.1:g.31842G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1467G= MANE Select ENSP00000416330.2:p.Gly489=
ENST00000442011.6:c.1467G= ENSP00000416330.2:p.Gly489=
ENST00000506699.5:n.1984G=
ENST00000507018.5:c.1445G=
ENST00000509485.5:c.382G=
ENST00000514242.5:n.238G=
ENST00000514554.5:c.619G=
NM_000358.2:c.1467G= NP_000349.1:p.Gly489=
NM_000358.3:c.1467G= MANE Select NP_000349.1:p.Gly489=