Canonical Allele Identifier: CA2336421032
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342036T= , CM000681.2:g.41342036T= GRCh38
NC_000019.9:g.41847941T= , CM000681.1:g.41847941T= GRCh37
NC_000019.8:g.46539781T= NCBI36
NG_013364.1:g.16891A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.713-6A= MANE Select ENSP00000221930.4:n.713-6A=
ENST00000600196.2:c.712+134A= ENSP00000504008.1:n.712+134A=
ENST00000677934.1:c.634+2711A= ENSP00000504769.1:n.634+2711A=
ENST00000221930.5:c.713-6A= ENSP00000221930.4:n.713-6A=
ENST00000597453.1:n.377A=
ENST00000600196.1:n.172+134A=
NM_000660.5:c.713-6A= NP_000651.3:n.713-6A=
XM_011527242.1:c.713-3A= XP_011525544.1:n.713-3A=
NM_000660.6:c.713-6A= NP_000651.3:n.713-6A=
XM_011527242.2:c.713-3A= XP_011525544.1:n.713-3A=
NM_000660.7:c.713-6A= MANE Select NP_000651.3:n.713-6A=