Canonical Allele Identifier: CA1584790994
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046334G= , CM000667.2:g.136046334G= GRCh38
NC_000005.9:g.135382023G= , CM000667.1:g.135382023G= GRCh37
NC_000005.8:g.135409922G= NCBI36
NG_012646.1:g.22440G=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-1G= MANE Select ENSP00000416330.2:n.299-1G=
ENST00000442011.6:c.299-1G= ENSP00000416330.2:n.299-1G=
ENST00000504185.5:n.456-1G=
ENST00000506699.5:n.364-1G=
ENST00000507018.5:c.216-1G=
ENST00000515433.1:n.590G=
NM_000358.2:c.299-1G= NP_000349.1:n.299-1G=
NM_000358.3:c.299-1G= MANE Select NP_000349.1:n.299-1G=