Canonical Allele Identifier: CA1584798701
Gene: TGFBI HGNC NCBI

Linked Data

dbSNP Id: rs1751657335

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136057095G>T , CM000667.2:g.136057095G>T GRCh38
NC_000005.9:g.135392784G>T , CM000667.1:g.135392784G>T GRCh37
NC_000005.8:g.135420683G>T NCBI36
NG_012646.1:g.33201G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1678+300G>T MANE Select ENSP00000416330.2:n.1678+300G>T
ENST00000442011.6:c.1678+300G>T ENSP00000416330.2:n.1678+300G>T
ENST00000506699.5:n.2195+300G>T
ENST00000507018.5:c.1656+300G>T
ENST00000509485.5:c.675+300G>T
ENST00000514242.5:n.449+300G>T
ENST00000514554.5:c.830+300G>T
NM_000358.2:c.1678+300G>T NP_000349.1:n.1678+300G>T
NM_000358.3:c.1678+300G>T MANE Select NP_000349.1:n.1678+300G>T