Canonical Allele Identifier: CA1584790978
Gene: TGFBI HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046312C= , CM000667.2:g.136046312C= GRCh38
NC_000005.9:g.135382001C= , CM000667.1:g.135382001C= GRCh37
NC_000005.8:g.135409900C= NCBI36
NG_012646.1:g.22418C=

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-23C= MANE Select ENSP00000416330.2:n.299-23C=
ENST00000442011.6:c.299-23C= ENSP00000416330.2:n.299-23C=
ENST00000504185.5:n.456-23C=
ENST00000506699.5:n.364-23C=
ENST00000507018.5:c.216-23C=
ENST00000515433.1:n.568C=
NM_000358.2:c.299-23C= NP_000349.1:n.299-23C=
NM_000358.3:c.299-23C= MANE Select NP_000349.1:n.299-23C=
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