Canonical Allele Identifier: CA1584790889
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1751422070

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046150T>A , CM000667.2:g.136046150T>A GRCh38
NC_000005.9:g.135381839T>A , CM000667.1:g.135381839T>A GRCh37
NC_000005.8:g.135409738T>A NCBI36
NG_012646.1:g.22256T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-185T>A MANE Select ENSP00000416330.2:n.299-185T>A
ENST00000442011.6:c.299-185T>A ENSP00000416330.2:n.299-185T>A
ENST00000504185.5:n.456-185T>A
ENST00000506699.5:n.364-185T>A
ENST00000507018.5:c.216-185T>A
ENST00000515433.1:n.406T>A
NM_000358.2:c.299-185T>A NP_000349.1:n.299-185T>A
NM_000358.3:c.299-185T>A MANE Select NP_000349.1:n.299-185T>A