Canonical Allele Identifier: CA2675393534
Gene: TGFBI HGNC NCBI

Linked Data

gnomAD v4: 5-136046175-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046175A>G , CM000667.2:g.136046175A>G GRCh38
NC_000005.9:g.135381864A>G , CM000667.1:g.135381864A>G GRCh37
NC_000005.8:g.135409763A>G NCBI36
NG_012646.1:g.22281A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-160A>G MANE Select ENSP00000416330.2:n.299-160A>G
ENST00000442011.6:c.299-160A>G ENSP00000416330.2:n.299-160A>G
ENST00000504185.5:n.456-160A>G
ENST00000506699.5:n.364-160A>G
ENST00000507018.5:c.216-160A>G
ENST00000515433.1:n.431A>G
NM_000358.2:c.299-160A>G NP_000349.1:n.299-160A>G
NM_000358.3:c.299-160A>G MANE Select NP_000349.1:n.299-160A>G
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