Canonical Allele Identifier: CA804305425
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1174933525
MyVariant Identifiers: chr5:g.135381748A>G (hg19) chr5:g.136046059A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046059A>G , CM000667.2:g.136046059A>G GRCh38
NC_000005.9:g.135381748A>G , CM000667.1:g.135381748A>G GRCh37
NC_000005.8:g.135409647A>G NCBI36
NG_012646.1:g.22165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-276A>G MANE Select ENSP00000416330.2:n.299-276A>G
ENST00000442011.6:c.299-276A>G ENSP00000416330.2:n.299-276A>G
ENST00000504185.5:n.456-276A>G
ENST00000506699.5:n.364-276A>G
ENST00000507018.5:c.216-276A>G
ENST00000515433.1:n.315A>G
NM_000358.2:c.299-276A>G NP_000349.1:n.299-276A>G
NM_000358.3:c.299-276A>G MANE Select NP_000349.1:n.299-276A>G
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