Canonical Allele Identifier: CA128059178
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs931145287
gnomAD v4: 5-136056921-A-C
MyVariant Identifiers: chr5:g.136056921A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136056921A>C , CM000667.2:g.136056921A>C GRCh38
NC_000005.9:g.135392610A>C , CM000667.1:g.135392610A>C GRCh37
NC_000005.8:g.135420509A>C NCBI36
NG_012646.1:g.33027A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1678+126A>C MANE Select ENSP00000416330.2:n.1678+126A>C
ENST00000442011.6:c.1678+126A>C ENSP00000416330.2:n.1678+126A>C
ENST00000506699.5:n.2195+126A>C
ENST00000507018.5:c.1656+126A>C
ENST00000509485.5:c.675+126A>C
ENST00000514242.5:n.449+126A>C
ENST00000514554.5:c.830+126A>C
NM_000358.2:c.1678+126A>C NP_000349.1:n.1678+126A>C
NM_000358.3:c.1678+126A>C MANE Select NP_000349.1:n.1678+126A>C
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