Canonical Allele Identifier: CA2336420976
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341906G= , CM000681.2:g.41341906G= GRCh38
NC_000019.9:g.41847811G= , CM000681.1:g.41847811G= GRCh37
NC_000019.8:g.46539651G= NCBI36
NG_013364.1:g.17021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.837C= MANE Select ENSP00000221930.4:p.Ala279=
ENST00000600196.2:c.712+264C= ENSP00000504008.1:n.712+264C=
ENST00000677934.1:c.634+2841C= ENSP00000504769.1:n.634+2841C=
ENST00000221930.5:c.837C= ENSP00000221930.4:p.Ala279=
ENST00000598758.5:c.125C=
ENST00000600196.1:n.172+264C=
NM_000660.5:c.837C= NP_000651.3:p.Ala279=
XM_011527242.1:c.840C= XP_011525544.1:p.Ala280=
NM_000660.6:c.837C= NP_000651.3:p.Ala279=
XM_011527242.2:c.840C= XP_011525544.1:p.Ala280=
NM_000660.7:c.837C= MANE Select NP_000651.3:p.Ala279=