Canonical Allele Identifier: CA2336420988
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341927T= , CM000681.2:g.41341927T= GRCh38
NC_000019.9:g.41847832T= , CM000681.1:g.41847832T= GRCh37
NC_000019.8:g.46539672T= NCBI36
NG_013364.1:g.17000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.816A= MANE Select ENSP00000221930.4:p.Gln272=
ENST00000600196.2:c.712+243A= ENSP00000504008.1:n.712+243A=
ENST00000677934.1:c.634+2820A= ENSP00000504769.1:n.634+2820A=
ENST00000221930.5:c.816A= ENSP00000221930.4:p.Gln272=
ENST00000598758.5:c.104A=
ENST00000600196.1:n.172+243A=
NM_000660.5:c.816A= NP_000651.3:p.Gln272=
XM_011527242.1:c.819A= XP_011525544.1:p.Gln273=
NM_000660.6:c.816A= NP_000651.3:p.Gln272=
XM_011527242.2:c.819A= XP_011525544.1:p.Gln273=
NM_000660.7:c.816A= MANE Select NP_000651.3:p.Gln272=