Canonical Allele Identifier: CA1584791100
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046550C= , CM000667.2:g.136046550C= GRCh38
NC_000005.9:g.135382239C= , CM000667.1:g.135382239C= GRCh37
NC_000005.8:g.135410138C= NCBI36
NG_012646.1:g.22656C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+55C= MANE Select ENSP00000416330.2:n.459+55C=
ENST00000442011.6:c.459+55C= ENSP00000416330.2:n.459+55C=
ENST00000506699.5:n.579C=
ENST00000507018.5:c.431C=
ENST00000515433.1:n.806C=
NM_000358.2:c.459+55C= NP_000349.1:n.459+55C=
NM_000358.3:c.459+55C= MANE Select NP_000349.1:n.459+55C=