Canonical Allele Identifier: CA1584791165
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046678G= , CM000667.2:g.136046678G= GRCh38
NC_000005.9:g.135382367G= , CM000667.1:g.135382367G= GRCh37
NC_000005.8:g.135410266G= NCBI36
NG_012646.1:g.22784G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.460-173G= MANE Select ENSP00000416330.2:n.460-173G=
ENST00000442011.6:c.460-173G= ENSP00000416330.2:n.460-173G=
ENST00000506699.5:n.707G=
ENST00000507018.5:c.437+122G=
ENST00000515433.1:n.934G=
NM_000358.2:c.460-173G= NP_000349.1:n.460-173G=
NM_000358.3:c.460-173G= MANE Select NP_000349.1:n.460-173G=