Canonical Allele Identifier: CA1584791020
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046398A= , CM000667.2:g.136046398A= GRCh38
NC_000005.9:g.135382087A= , CM000667.1:g.135382087A= GRCh37
NC_000005.8:g.135409986A= NCBI36
NG_012646.1:g.22504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.362A= MANE Select ENSP00000416330.2:p.Tyr121=
ENST00000442011.6:c.362A= ENSP00000416330.2:p.Tyr121=
ENST00000504185.5:n.519A=
ENST00000506699.5:n.427A=
ENST00000507018.5:c.279A=
ENST00000515433.1:n.654A=
NM_000358.2:c.362A= NP_000349.1:p.Tyr121=
NM_000358.3:c.362A= MANE Select NP_000349.1:p.Tyr121=