Canonical Allele Identifier: CA1221568403
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218441336A= , CM000663.2:g.218441336A= GRCh38
NC_000001.10:g.218614678A= , CM000663.1:g.218614678A= GRCh37
NC_000001.9:g.216681301A= NCBI36
NG_027721.1:g.101003A=
NG_027721.2:g.101003A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.1219A= MANE Select ENSP00000355897.4:p.Ile407=
ENST00000366929.4:c.1303A= ENSP00000355896.4:p.Ile435=
ENST00000366930.8:c.1219A= ENSP00000355897.4:p.Ile407=
ENST00000479322.1:n.703A=
NM_001135599.2:c.1303A= NP_001129071.1:p.Ile435=
NM_003238.3:c.1219A= NP_003229.1:p.Ile407=
NM_001135599.3:c.1303A= NP_001129071.1:p.Ile435=
NM_003238.4:c.1219A= NP_003229.1:p.Ile407=
NR_138148.1:n.2522A=
NR_138149.1:n.2606A=
NM_003238.5:c.1219A= NP_003229.1:p.Ile407=
NM_003238.6:c.1219A= MANE Select NP_003229.1:p.Ile407=
NM_001135599.4:c.1303A= NP_001129071.1:p.Ile435=
NR_138148.2:n.2470A=
NR_138149.2:n.2554A=