Canonical Allele Identifier: CA446551043
Gene: TGFBI HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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