Canonical Allele Identifier: CA1584796906
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136055677C= , CM000667.2:g.136055677C= GRCh38
NC_000005.9:g.135391366C= , CM000667.1:g.135391366C= GRCh37
NC_000005.8:g.135419265C= NCBI36
NG_012646.1:g.31783C=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.1411-3C= MANE Select ENSP00000416330.2:n.1411-3C=
ENST00000442011.6:c.1411-3C= ENSP00000416330.2:n.1411-3C=
ENST00000506699.5:n.1928-3C=
ENST00000507018.5:c.1389-3C=
ENST00000509485.5:c.326-3C=
ENST00000514242.5:n.179C=
ENST00000514554.5:c.563-3C=
NM_000358.2:c.1411-3C= NP_000349.1:n.1411-3C=
NM_000358.3:c.1411-3C= MANE Select NP_000349.1:n.1411-3C=
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