Canonical Allele Identifier: CA361032689
Gene: TGFBI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046418C>A , CM000667.2:g.136046418C>A GRCh38
NC_000005.9:g.135382107C>A , CM000667.1:g.135382107C>A GRCh37
NC_000005.8:g.135410006C>A NCBI36
NG_012646.1:g.22524C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.382C>A MANE Select ENSP00000416330.2:p.Leu128Met
ENST00000442011.6:c.382C>A ENSP00000416330.2:p.Leu128Met
ENST00000504185.5:n.539C>A
ENST00000506699.5:n.447C>A
ENST00000507018.5:c.299C>A
ENST00000515433.1:n.674C>A
NM_000358.2:c.382C>A NP_000349.1:p.Leu128Met
NM_000358.3:c.382C>A MANE Select NP_000349.1:p.Leu128Met