Canonical Allele Identifier: CA2336423828
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348064G= , CM000681.2:g.41348064G= GRCh38
NC_000019.9:g.41853969G= , CM000681.1:g.41853969G= GRCh37
NC_000019.8:g.46545809G= NCBI36
NG_013364.1:g.10863C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.516+231C= MANE Select ENSP00000221930.4:n.516+231C=
ENST00000600196.2:c.516+231C= ENSP00000504008.1:n.516+231C=
ENST00000677934.1:c.516+231C= ENSP00000504769.1:n.516+231C=
ENST00000221930.5:c.516+231C= ENSP00000221930.4:n.516+231C=
ENST00000597453.1:n.47+231C=
NM_000660.5:c.516+231C= NP_000651.3:n.516+231C=
XM_011527242.1:c.516+231C= XP_011525544.1:n.516+231C=
NM_000660.6:c.516+231C= NP_000651.3:n.516+231C=
XM_011527242.2:c.516+231C= XP_011525544.1:n.516+231C=
NM_000660.7:c.516+231C= MANE Select NP_000651.3:n.516+231C=