Canonical Allele Identifier: CA1584791142
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1751433531
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046622del , CM000667.2:g.136046622del GRCh38
NC_000005.9:g.135382311del , CM000667.1:g.135382311del GRCh37
NC_000005.8:g.135410210del NCBI36
NG_012646.1:g.22728del

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+127del MANE Select ENSP00000416330.2:n.459+127del
ENST00000442011.6:c.459+127del ENSP00000416330.2:n.459+127del
ENST00000506699.5:n.651del
ENST00000507018.5:c.437+66del
ENST00000515433.1:n.878del
NM_000358.2:c.459+127del NP_000349.1:n.459+127del
NM_000358.3:c.459+127del MANE Select NP_000349.1:n.459+127del
Search 100 bp 5'
Search 100 bp 3'