Canonical Allele Identifier: CA1584791131
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1751432947
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046602G>C , CM000667.2:g.136046602G>C GRCh38
NC_000005.9:g.135382291G>C , CM000667.1:g.135382291G>C GRCh37
NC_000005.8:g.135410190G>C NCBI36
NG_012646.1:g.22708G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+107G>C MANE Select ENSP00000416330.2:n.459+107G>C
ENST00000442011.6:c.459+107G>C ENSP00000416330.2:n.459+107G>C
ENST00000506699.5:n.631G>C
ENST00000507018.5:c.437+46G>C
ENST00000515433.1:n.858G>C
NM_000358.2:c.459+107G>C NP_000349.1:n.459+107G>C
NM_000358.3:c.459+107G>C MANE Select NP_000349.1:n.459+107G>C
Search 100 bp 5'
Search 100 bp 3'