Canonical Allele Identifier: CA1584791164
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046676A= , CM000667.2:g.136046676A= GRCh38
NC_000005.9:g.135382365A= , CM000667.1:g.135382365A= GRCh37
NC_000005.8:g.135410264A= NCBI36
NG_012646.1:g.22782A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.460-175A= MANE Select ENSP00000416330.2:n.460-175A=
ENST00000442011.6:c.460-175A= ENSP00000416330.2:n.460-175A=
ENST00000506699.5:n.705A=
ENST00000507018.5:c.437+120A=
ENST00000515433.1:n.932A=
NM_000358.2:c.460-175A= NP_000349.1:n.460-175A=
NM_000358.3:c.460-175A= MANE Select NP_000349.1:n.460-175A=