Canonical Allele Identifier: CA1584790850
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046042C= , CM000667.2:g.136046042C= GRCh38
NC_000005.9:g.135381731C= , CM000667.1:g.135381731C= GRCh37
NC_000005.8:g.135409630C= NCBI36
NG_012646.1:g.22148C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-293C= MANE Select ENSP00000416330.2:n.299-293C=
ENST00000442011.6:c.299-293C= ENSP00000416330.2:n.299-293C=
ENST00000504185.5:n.456-293C=
ENST00000506699.5:n.364-293C=
ENST00000507018.5:c.216-293C=
ENST00000515433.1:n.298C=
NM_000358.2:c.299-293C= NP_000349.1:n.299-293C=
NM_000358.3:c.299-293C= MANE Select NP_000349.1:n.299-293C=