Canonical Allele Identifier: CA2336421281
Gene: TGFB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342471T= , CM000681.2:g.41342471T= GRCh38
NC_000019.9:g.41848376T= , CM000681.1:g.41848376T= GRCh37
NC_000019.8:g.46540216T= NCBI36
NG_013364.1:g.16456A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-224A= MANE Select ENSP00000221930.4:n.635-224A=
ENST00000600196.2:c.635-224A= ENSP00000504008.1:n.635-224A=
ENST00000677934.1:c.634+2276A= ENSP00000504769.1:n.634+2276A=
ENST00000221930.5:c.635-224A= ENSP00000221930.4:n.635-224A=
ENST00000597453.1:n.166-224A=
ENST00000600196.1:n.95-224A=
NM_000660.5:c.635-224A= NP_000651.3:n.635-224A=
XM_011527242.1:c.635-224A= XP_011525544.1:n.635-224A=
NM_000660.6:c.635-224A= NP_000651.3:n.635-224A=
XM_011527242.2:c.635-224A= XP_011525544.1:n.635-224A=
NM_000660.7:c.635-224A= MANE Select NP_000651.3:n.635-224A=
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