Canonical Allele Identifier: CA2814427052
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342341T>G , CM000681.2:g.41342341T>G GRCh38
NC_000019.9:g.41848246T>G , CM000681.1:g.41848246T>G GRCh37
NC_000019.8:g.46540086T>G NCBI36
NG_013364.1:g.16586A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-94A>C MANE Select ENSP00000221930.4:n.635-94A>C
ENST00000600196.2:c.635-94A>C ENSP00000504008.1:n.635-94A>C
ENST00000677934.1:c.634+2406A>C ENSP00000504769.1:n.634+2406A>C
ENST00000221930.5:c.635-94A>C ENSP00000221930.4:n.635-94A>C
ENST00000597453.1:n.166-94A>C
ENST00000600196.1:n.95-94A>C
NM_000660.5:c.635-94A>C NP_000651.3:n.635-94A>C
XM_011527242.1:c.635-94A>C XP_011525544.1:n.635-94A>C
NM_000660.6:c.635-94A>C NP_000651.3:n.635-94A>C
XM_011527242.2:c.635-94A>C XP_011525544.1:n.635-94A>C
NM_000660.7:c.635-94A>C MANE Select NP_000651.3:n.635-94A>C