Canonical Allele Identifier: CA804305485
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1205470044
MyVariant Identifiers: chr5:g.135381893C>G (hg19) chr5:g.136046204C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046204C>G , CM000667.2:g.136046204C>G GRCh38
NC_000005.9:g.135381893C>G , CM000667.1:g.135381893C>G GRCh37
NC_000005.8:g.135409792C>G NCBI36
NG_012646.1:g.22310C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.299-131C>G MANE Select ENSP00000416330.2:n.299-131C>G
ENST00000442011.6:c.299-131C>G ENSP00000416330.2:n.299-131C>G
ENST00000504185.5:n.456-131C>G
ENST00000506699.5:n.364-131C>G
ENST00000507018.5:c.216-131C>G
ENST00000515433.1:n.460C>G
NM_000358.2:c.299-131C>G NP_000349.1:n.299-131C>G
NM_000358.3:c.299-131C>G MANE Select NP_000349.1:n.299-131C>G
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