Canonical Allele Identifier: CA2336420979
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341912G= , CM000681.2:g.41341912G= GRCh38
NC_000019.9:g.41847817G= , CM000681.1:g.41847817G= GRCh37
NC_000019.8:g.46539657G= NCBI36
NG_013364.1:g.17015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.831C= MANE Select ENSP00000221930.4:p.Arg277=
ENST00000600196.2:c.712+258C= ENSP00000504008.1:n.712+258C=
ENST00000677934.1:c.634+2835C= ENSP00000504769.1:n.634+2835C=
ENST00000221930.5:c.831C= ENSP00000221930.4:p.Arg277=
ENST00000598758.5:c.119C=
ENST00000600196.1:n.172+258C=
NM_000660.5:c.831C= NP_000651.3:p.Arg277=
XM_011527242.1:c.834C= XP_011525544.1:p.Arg278=
NM_000660.6:c.831C= NP_000651.3:p.Arg277=
XM_011527242.2:c.834C= XP_011525544.1:p.Arg278=
NM_000660.7:c.831C= MANE Select NP_000651.3:p.Arg277=