Canonical Allele Identifier: CA1584798287
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136056738G= , CM000667.2:g.136056738G= GRCh38
NC_000005.9:g.135392427G= , CM000667.1:g.135392427G= GRCh37
NC_000005.8:g.135420326G= NCBI36
NG_012646.1:g.32844G=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.1621G= MANE Select ENSP00000416330.2:p.Ala541=
ENST00000442011.6:c.1621G= ENSP00000416330.2:p.Ala541=
ENST00000506699.5:n.2138G=
ENST00000507018.5:c.1599G=
ENST00000509485.5:c.618G=
ENST00000514242.5:n.392G=
ENST00000514554.5:c.773G=
NM_000358.2:c.1621G= NP_000349.1:p.Ala541=
NM_000358.3:c.1621G= MANE Select NP_000349.1:p.Ala541=