Canonical Allele Identifier: CA2336420986
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341924G= , CM000681.2:g.41341924G= GRCh38
NC_000019.9:g.41847829G= , CM000681.1:g.41847829G= GRCh37
NC_000019.8:g.46539669G= NCBI36
NG_013364.1:g.17003C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.819C= MANE Select ENSP00000221930.4:p.Ser273=
ENST00000600196.2:c.712+246C= ENSP00000504008.1:n.712+246C=
ENST00000677934.1:c.634+2823C= ENSP00000504769.1:n.634+2823C=
ENST00000221930.5:c.819C= ENSP00000221930.4:p.Ser273=
ENST00000598758.5:c.107C=
ENST00000600196.1:n.172+246C=
NM_000660.5:c.819C= NP_000651.3:p.Ser273=
XM_011527242.1:c.822C= XP_011525544.1:p.Ser274=
NM_000660.6:c.819C= NP_000651.3:p.Ser273=
XM_011527242.2:c.822C= XP_011525544.1:p.Ser274=
NM_000660.7:c.819C= MANE Select NP_000651.3:p.Ser273=