Canonical Allele Identifier: CA1584790982
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046319T= , CM000667.2:g.136046319T= GRCh38
NC_000005.9:g.135382008T= , CM000667.1:g.135382008T= GRCh37
NC_000005.8:g.135409907T= NCBI36
NG_012646.1:g.22425T=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-16T= MANE Select ENSP00000416330.2:n.299-16T=
ENST00000442011.6:c.299-16T= ENSP00000416330.2:n.299-16T=
ENST00000504185.5:n.456-16T=
ENST00000506699.5:n.364-16T=
ENST00000507018.5:c.216-16T=
ENST00000515433.1:n.575T=
NM_000358.2:c.299-16T= NP_000349.1:n.299-16T=
NM_000358.3:c.299-16T= MANE Select NP_000349.1:n.299-16T=