Canonical Allele Identifier: CA2675393768
Gene: TGFBI HGNC NCBI

Linked Data

gnomAD v4: 5-136046677-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046677T>C , CM000667.2:g.136046677T>C GRCh38
NC_000005.9:g.135382366T>C , CM000667.1:g.135382366T>C GRCh37
NC_000005.8:g.135410265T>C NCBI36
NG_012646.1:g.22783T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.460-174T>C MANE Select ENSP00000416330.2:n.460-174T>C
ENST00000442011.6:c.460-174T>C ENSP00000416330.2:n.460-174T>C
ENST00000506699.5:n.706T>C
ENST00000507018.5:c.437+121T>C
ENST00000515433.1:n.933T>C
NM_000358.2:c.460-174T>C NP_000349.1:n.460-174T>C
NM_000358.3:c.460-174T>C MANE Select NP_000349.1:n.460-174T>C
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