Canonical Allele Identifier: CA1221565868
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218437240A= , CM000663.2:g.218437240A= GRCh38
NC_000001.10:g.218610582A= , CM000663.1:g.218610582A= GRCh37
NC_000001.9:g.216677205A= NCBI36
NG_027721.1:g.96907A=
NG_027721.2:g.96907A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366930.9:c.933-103A= MANE Select ENSP00000355897.4:n.933-103A=
ENST00000366929.4:c.1017-103A= ENSP00000355896.4:n.1017-103A=
ENST00000366930.8:c.933-103A= ENSP00000355897.4:n.933-103A=
ENST00000479322.1:n.417-103A=
NM_001135599.2:c.1017-103A= NP_001129071.1:n.1017-103A=
NM_003238.3:c.933-103A= NP_003229.1:n.933-103A=
NM_001135599.3:c.1017-103A= NP_001129071.1:n.1017-103A=
NM_003238.4:c.933-103A= NP_003229.1:n.933-103A=
NR_138148.1:n.2236-103A=
NR_138149.1:n.2320-103A=
NM_003238.5:c.933-103A= NP_003229.1:n.933-103A=
NM_003238.6:c.933-103A= MANE Select NP_003229.1:n.933-103A=
NM_001135599.4:c.1017-103A= NP_001129071.1:n.1017-103A=
NR_138148.2:n.2184-103A=
NR_138149.2:n.2268-103A=