Canonical Allele Identifier: CA2768528833
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046183A>G , CM000667.2:g.136046183A>G GRCh38
NC_000005.9:g.135381872A>G , CM000667.1:g.135381872A>G GRCh37
NC_000005.8:g.135409771A>G NCBI36
NG_012646.1:g.22289A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-152A>G MANE Select ENSP00000416330.2:n.299-152A>G
ENST00000442011.6:c.299-152A>G ENSP00000416330.2:n.299-152A>G
ENST00000504185.5:n.456-152A>G
ENST00000506699.5:n.364-152A>G
ENST00000507018.5:c.216-152A>G
ENST00000515433.1:n.439A>G
NM_000358.2:c.299-152A>G NP_000349.1:n.299-152A>G
NM_000358.3:c.299-152A>G MANE Select NP_000349.1:n.299-152A>G