Canonical Allele Identifier: CA1584790985
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1751425210

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136046325G>C , CM000667.2:g.136046325G>C GRCh38
NC_000005.9:g.135382014G>C , CM000667.1:g.135382014G>C GRCh37
NC_000005.8:g.135409913G>C NCBI36
NG_012646.1:g.22431G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.299-10G>C MANE Select ENSP00000416330.2:n.299-10G>C
ENST00000442011.6:c.299-10G>C ENSP00000416330.2:n.299-10G>C
ENST00000504185.5:n.456-10G>C
ENST00000506699.5:n.364-10G>C
ENST00000507018.5:c.216-10G>C
ENST00000515433.1:n.581G>C
NM_000358.2:c.299-10G>C NP_000349.1:n.299-10G>C
NM_000358.3:c.299-10G>C MANE Select NP_000349.1:n.299-10G>C