Canonical Allele Identifier: CA361032413
Gene: TGFBI HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135382022A>C (hg19) chr5:g.136046333A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046333A>C , CM000667.2:g.136046333A>C GRCh38
NC_000005.9:g.135382022A>C , CM000667.1:g.135382022A>C GRCh37
NC_000005.8:g.135409921A>C NCBI36
NG_012646.1:g.22439A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-2A>C MANE Select ENSP00000416330.2:n.299-2A>C
ENST00000442011.6:c.299-2A>C ENSP00000416330.2:n.299-2A>C
ENST00000504185.5:n.456-2A>C
ENST00000506699.5:n.364-2A>C
ENST00000507018.5:c.216-2A>C
ENST00000515433.1:n.589A>C
NM_000358.2:c.299-2A>C NP_000349.1:n.299-2A>C
NM_000358.3:c.299-2A>C MANE Select NP_000349.1:n.299-2A>C
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