Canonical Allele Identifier: CA2675393648
Gene: TGFBI HGNC NCBI

Linked Data

gnomAD v4: 5-136046535-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046535A>G , CM000667.2:g.136046535A>G GRCh38
NC_000005.9:g.135382224A>G , CM000667.1:g.135382224A>G GRCh37
NC_000005.8:g.135410123A>G NCBI36
NG_012646.1:g.22641A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+40A>G MANE Select ENSP00000416330.2:n.459+40A>G
ENST00000442011.6:c.459+40A>G ENSP00000416330.2:n.459+40A>G
ENST00000506699.5:n.564A>G
ENST00000507018.5:c.416A>G
ENST00000515433.1:n.791A>G
NM_000358.2:c.459+40A>G NP_000349.1:n.459+40A>G
NM_000358.3:c.459+40A>G MANE Select NP_000349.1:n.459+40A>G
Search 100 bp 5'
Search 100 bp 3'