Canonical Allele Identifier: CA446550999

Gene: TGFBI

Linked Data

• MyVariant Identifiers: chr5:g.135382052C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.136046363C>G , CM000667.2:g.136046363C>G	GRCh38
NC_000005.9:g.135382052C>G , CM000667.1:g.135382052C>G	GRCh37
NC_000005.8:g.135409951C>G	NCBI36
NG_012646.1:g.22469C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442011.7:c.327C>G MANE Select	ENSP00000416330.2:p.Thr109=
ENST00000442011.6:c.327C>G	ENSP00000416330.2:p.Thr109=
ENST00000504185.5:n.484C>G
ENST00000506699.5:n.392C>G
ENST00000507018.5:c.244C>G
ENST00000515433.1:n.619C>G
NM_000358.2:c.327C>G	NP_000349.1:p.Thr109=
NM_000358.3:c.327C>G MANE Select	NP_000349.1:p.Thr109=