Canonical Allele Identifier: CA2675393774
Gene: TGFBI HGNC NCBI

Linked Data

gnomAD v4: 5-136046681-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046681C>G , CM000667.2:g.136046681C>G GRCh38
NC_000005.9:g.135382370C>G , CM000667.1:g.135382370C>G GRCh37
NC_000005.8:g.135410269C>G NCBI36
NG_012646.1:g.22787C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.460-170C>G MANE Select ENSP00000416330.2:n.460-170C>G
ENST00000442011.6:c.460-170C>G ENSP00000416330.2:n.460-170C>G
ENST00000506699.5:n.710C>G
ENST00000507018.5:c.437+125C>G
ENST00000515433.1:n.937C>G
NM_000358.2:c.460-170C>G NP_000349.1:n.460-170C>G
NM_000358.3:c.460-170C>G MANE Select NP_000349.1:n.460-170C>G
Search 100 bp 5'
Search 100 bp 3'