Canonical Allele Identifier: CA1221528718
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346975G= , CM000663.2:g.218346975G= GRCh38
NC_000001.10:g.218520317G= , CM000663.1:g.218520317G= GRCh37
NC_000001.9:g.216586940G= NCBI36
NG_027721.1:g.6642G=
NG_027721.2:g.6642G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.274G= MANE Select ENSP00000355897.4:p.Glu92=
ENST00000366929.4:c.274G= ENSP00000355896.4:p.Glu92=
ENST00000366930.8:c.274G= ENSP00000355897.4:p.Glu92=
NM_001135599.2:c.274G= NP_001129071.1:p.Glu92=
NM_003238.3:c.274G= NP_003229.1:p.Glu92=
NM_001135599.3:c.274G= NP_001129071.1:p.Glu92=
NM_003238.4:c.274G= NP_003229.1:p.Glu92=
NR_138148.1:n.1692G=
NR_138149.1:n.1692G=
NM_003238.5:c.274G= NP_003229.1:p.Glu92=
NM_003238.6:c.274G= MANE Select NP_003229.1:p.Glu92=
NM_001135599.4:c.274G= NP_001129071.1:p.Glu92=
NR_138148.2:n.1640G=
NR_138149.2:n.1640G=