Canonical Allele Identifier: CA361032672
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs372436914

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046410C>A , CM000667.2:g.136046410C>A GRCh38
NC_000005.9:g.135382099C>A , CM000667.1:g.135382099C>A GRCh37
NC_000005.8:g.135409998C>A NCBI36
NG_012646.1:g.22516C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.374C>A MANE Select ENSP00000416330.2:p.Thr125Lys
ENST00000442011.6:c.374C>A ENSP00000416330.2:p.Thr125Lys
ENST00000504185.5:n.531C>A
ENST00000506699.5:n.439C>A
ENST00000507018.5:c.291C>A
ENST00000515433.1:n.666C>A
NM_000358.2:c.374C>A NP_000349.1:p.Thr125Lys
NM_000358.3:c.374C>A MANE Select NP_000349.1:p.Thr125Lys