Canonical Allele Identifier: CA446551035
Gene: TGFBI HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135382097C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046408C>G , CM000667.2:g.136046408C>G GRCh38
NC_000005.9:g.135382097C>G , CM000667.1:g.135382097C>G GRCh37
NC_000005.8:g.135409996C>G NCBI36
NG_012646.1:g.22514C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.372C>G MANE Select ENSP00000416330.2:p.Arg124=
ENST00000442011.6:c.372C>G ENSP00000416330.2:p.Arg124=
ENST00000504185.5:n.529C>G
ENST00000506699.5:n.437C>G
ENST00000507018.5:c.289C>G
ENST00000515433.1:n.664C>G
NM_000358.2:c.372C>G NP_000349.1:p.Arg124=
NM_000358.3:c.372C>G MANE Select NP_000349.1:p.Arg124=