Canonical Allele Identifier: CA361041836
Gene: TGFBI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136056744A>T , CM000667.2:g.136056744A>T GRCh38
NC_000005.9:g.135392433A>T , CM000667.1:g.135392433A>T GRCh37
NC_000005.8:g.135420332A>T NCBI36
NG_012646.1:g.32850A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.1627A>T MANE Select ENSP00000416330.2:p.Thr543Ser
ENST00000442011.6:c.1627A>T ENSP00000416330.2:p.Thr543Ser
ENST00000506699.5:n.2144A>T
ENST00000507018.5:c.1605A>T
ENST00000509485.5:c.624A>T
ENST00000514242.5:n.398A>T
ENST00000514554.5:c.779A>T
NM_000358.2:c.1627A>T NP_000349.1:p.Thr543Ser
NM_000358.3:c.1627A>T MANE Select NP_000349.1:p.Thr543Ser