Canonical Allele Identifier: CA2675393465
Gene: TGFBI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046076C>T , CM000667.2:g.136046076C>T GRCh38
NC_000005.9:g.135381765C>T , CM000667.1:g.135381765C>T GRCh37
NC_000005.8:g.135409664C>T NCBI36
NG_012646.1:g.22182C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-259C>T MANE Select ENSP00000416330.2:n.299-259C>T
ENST00000442011.6:c.299-259C>T ENSP00000416330.2:n.299-259C>T
ENST00000504185.5:n.456-259C>T
ENST00000506699.5:n.364-259C>T
ENST00000507018.5:c.216-259C>T
ENST00000515433.1:n.332C>T
NM_000358.2:c.299-259C>T NP_000349.1:n.299-259C>T
NM_000358.3:c.299-259C>T MANE Select NP_000349.1:n.299-259C>T