Canonical Allele Identifier: CA2336421146
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342247C= , CM000681.2:g.41342247C= GRCh38
NC_000019.9:g.41848152C= , CM000681.1:g.41848152C= GRCh37
NC_000019.8:g.46539992C= NCBI36
NG_013364.1:g.16680G=

Transcript Alleles

HGVS Amino-acid change
ENST00000221930.6:c.635G= MANE Select ENSP00000221930.4:p.Gly212=
ENST00000600196.2:c.635G= ENSP00000504008.1:p.Gly212=
ENST00000677934.1:c.634+2500G= ENSP00000504769.1:n.634+2500G=
ENST00000221930.5:c.635G= ENSP00000221930.4:p.Gly212=
ENST00000597453.1:n.166G=
ENST00000600196.1:n.95G=
NM_000660.5:c.635G= NP_000651.3:p.Gly212=
XM_011527242.1:c.635G= XP_011525544.1:p.Gly212=
NM_000660.6:c.635G= NP_000651.3:p.Gly212=
XM_011527242.2:c.635G= XP_011525544.1:p.Gly212=
NM_000660.7:c.635G= MANE Select NP_000651.3:p.Gly212=