Canonical Allele Identifier: CA2849098763
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41348085T>C , CM000681.2:g.41348085T>C GRCh38
NC_000019.9:g.41853990T>C , CM000681.1:g.41853990T>C GRCh37
NC_000019.8:g.46545830T>C NCBI36
NG_013364.1:g.10842A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.516+210A>G MANE Select ENSP00000221930.4:n.516+210A>G
ENST00000600196.2:c.516+210A>G ENSP00000504008.1:n.516+210A>G
ENST00000677934.1:c.516+210A>G ENSP00000504769.1:n.516+210A>G
ENST00000221930.5:c.516+210A>G ENSP00000221930.4:n.516+210A>G
ENST00000597453.1:n.47+210A>G
NM_000660.5:c.516+210A>G NP_000651.3:n.516+210A>G
XM_011527242.1:c.516+210A>G XP_011525544.1:n.516+210A>G
NM_000660.6:c.516+210A>G NP_000651.3:n.516+210A>G
XM_011527242.2:c.516+210A>G XP_011525544.1:n.516+210A>G
NM_000660.7:c.516+210A>G MANE Select NP_000651.3:n.516+210A>G