Canonical Allele Identifier: CA446551042
Gene: TGFBI HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135382109G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046420G>C , CM000667.2:g.136046420G>C GRCh38
NC_000005.9:g.135382109G>C , CM000667.1:g.135382109G>C GRCh37
NC_000005.8:g.135410008G>C NCBI36
NG_012646.1:g.22526G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.384G>C MANE Select ENSP00000416330.2:p.Leu128=
ENST00000442011.6:c.384G>C ENSP00000416330.2:p.Leu128=
ENST00000504185.5:n.541G>C
ENST00000506699.5:n.449G>C
ENST00000507018.5:c.301G>C
ENST00000515433.1:n.676G>C
NM_000358.2:c.384G>C NP_000349.1:p.Leu128=
NM_000358.3:c.384G>C MANE Select NP_000349.1:p.Leu128=