Canonical Allele Identifier: CA804298852
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1219023019
MyVariant Identifiers: chr5:g.135392747A>C (hg19) chr5:g.136057058A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136057058A>C , CM000667.2:g.136057058A>C GRCh38
NC_000005.9:g.135392747A>C , CM000667.1:g.135392747A>C GRCh37
NC_000005.8:g.135420646A>C NCBI36
NG_012646.1:g.33164A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1678+263A>C MANE Select ENSP00000416330.2:n.1678+263A>C
ENST00000442011.6:c.1678+263A>C ENSP00000416330.2:n.1678+263A>C
ENST00000506699.5:n.2195+263A>C
ENST00000507018.5:c.1656+263A>C
ENST00000509485.5:c.675+263A>C
ENST00000514242.5:n.449+263A>C
ENST00000514554.5:c.830+263A>C
NM_000358.2:c.1678+263A>C NP_000349.1:n.1678+263A>C
NM_000358.3:c.1678+263A>C MANE Select NP_000349.1:n.1678+263A>C
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