Canonical Allele Identifier: CA1584790995
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046336C= , CM000667.2:g.136046336C= GRCh38
NC_000005.9:g.135382025C= , CM000667.1:g.135382025C= GRCh37
NC_000005.8:g.135409924C= NCBI36
NG_012646.1:g.22442C=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.300C= MANE Select ENSP00000416330.2:p.Ala100=
ENST00000442011.6:c.300C= ENSP00000416330.2:p.Ala100=
ENST00000504185.5:n.457C=
ENST00000506699.5:n.365C=
ENST00000507018.5:c.217C=
ENST00000515433.1:n.592C=
NM_000358.2:c.300C= NP_000349.1:p.Ala100=
NM_000358.3:c.300C= MANE Select NP_000349.1:p.Ala100=