Canonical Allele Identifier: CA361032742
Gene: TGFBI HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.135382132G>C (hg19) chr5:g.136046443G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046443G>C , CM000667.2:g.136046443G>C GRCh38
NC_000005.9:g.135382132G>C , CM000667.1:g.135382132G>C GRCh37
NC_000005.8:g.135410031G>C NCBI36
NG_012646.1:g.22549G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.407G>C MANE Select ENSP00000416330.2:p.Gly136Ala
ENST00000442011.6:c.407G>C ENSP00000416330.2:p.Gly136Ala
ENST00000506699.5:n.472G>C
ENST00000507018.5:c.324G>C
ENST00000515433.1:n.699G>C
NM_000358.2:c.407G>C NP_000349.1:p.Gly136Ala
NM_000358.3:c.407G>C MANE Select NP_000349.1:p.Gly136Ala
Search 100 bp 5'
Search 100 bp 3'