Canonical Allele Identifier: CA1140904765
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218437340C= , CM000663.2:g.218437340C= GRCh38
NC_000001.10:g.218610682C= , CM000663.1:g.218610682C= GRCh37
NC_000001.9:g.216677305C= NCBI36
NG_027721.1:g.97007C=
NG_027721.2:g.97007C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366930.9:c.933-3C= MANE Select ENSP00000355897.4:n.933-3C=
ENST00000366929.4:c.1017-3C= ENSP00000355896.4:n.1017-3C=
ENST00000366930.8:c.933-3C= ENSP00000355897.4:n.933-3C=
ENST00000479322.1:n.417-3C=
NM_001135599.2:c.1017-3C= NP_001129071.1:n.1017-3C=
NM_003238.3:c.933-3C= NP_003229.1:n.933-3C=
NM_001135599.3:c.1017-3C= NP_001129071.1:n.1017-3C=
NM_003238.4:c.933-3C= NP_003229.1:n.933-3C=
NR_138148.1:n.2236-3C=
NR_138149.1:n.2320-3C=
NM_003238.5:c.933-3C= NP_003229.1:n.933-3C=
NM_003238.6:c.933-3C= MANE Select NP_003229.1:n.933-3C=
NM_001135599.4:c.1017-3C= NP_001129071.1:n.1017-3C=
NR_138148.2:n.2184-3C=
NR_138149.2:n.2268-3C=