Canonical Allele Identifier: CA2675393461
Gene: TGFBI HGNC NCBI

Linked Data

gnomAD v4: 5-136046072-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046072A>C , CM000667.2:g.136046072A>C GRCh38
NC_000005.9:g.135381761A>C , CM000667.1:g.135381761A>C GRCh37
NC_000005.8:g.135409660A>C NCBI36
NG_012646.1:g.22178A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-263A>C MANE Select ENSP00000416330.2:n.299-263A>C
ENST00000442011.6:c.299-263A>C ENSP00000416330.2:n.299-263A>C
ENST00000504185.5:n.456-263A>C
ENST00000506699.5:n.364-263A>C
ENST00000507018.5:c.216-263A>C
ENST00000515433.1:n.328A>C
NM_000358.2:c.299-263A>C NP_000349.1:n.299-263A>C
NM_000358.3:c.299-263A>C MANE Select NP_000349.1:n.299-263A>C
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