Canonical Allele Identifier: CA2675397123
Gene: TGFBI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136055597C>T , CM000667.2:g.136055597C>T GRCh38
NC_000005.9:g.135391286C>T , CM000667.1:g.135391286C>T GRCh37
NC_000005.8:g.135419185C>T NCBI36
NG_012646.1:g.31703C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000442011.7:c.1411-83C>T MANE Select ENSP00000416330.2:n.1411-83C>T
ENST00000442011.6:c.1411-83C>T ENSP00000416330.2:n.1411-83C>T
ENST00000506699.5:n.1928-83C>T
ENST00000507018.5:c.1389-83C>T
ENST00000509485.5:c.326-83C>T
ENST00000514242.5:n.99C>T
ENST00000514554.5:c.563-83C>T
NM_000358.2:c.1411-83C>T NP_000349.1:n.1411-83C>T
NM_000358.3:c.1411-83C>T MANE Select NP_000349.1:n.1411-83C>T