Canonical Allele Identifier: CA2675393732
Gene: TGFBI HGNC NCBI

Linked Data

gnomAD v4: 5-136046632-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046632G>A , CM000667.2:g.136046632G>A GRCh38
NC_000005.9:g.135382321G>A , CM000667.1:g.135382321G>A GRCh37
NC_000005.8:g.135410220G>A NCBI36
NG_012646.1:g.22738G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.459+137G>A MANE Select ENSP00000416330.2:n.459+137G>A
ENST00000442011.6:c.459+137G>A ENSP00000416330.2:n.459+137G>A
ENST00000506699.5:n.661G>A
ENST00000507018.5:c.437+76G>A
ENST00000515433.1:n.888G>A
NM_000358.2:c.459+137G>A NP_000349.1:n.459+137G>A
NM_000358.3:c.459+137G>A MANE Select NP_000349.1:n.459+137G>A
Search 100 bp 5'
Search 100 bp 3'