Canonical Allele Identifier: CA1221528628
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346746C= , CM000663.2:g.218346746C= GRCh38
NC_000001.10:g.218520088C= , CM000663.1:g.218520088C= GRCh37
NC_000001.9:g.216586711C= NCBI36
NG_027721.1:g.6413C=
NG_027721.2:g.6413C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.45C= MANE Select ENSP00000355897.4:p.Val15=
ENST00000366929.4:c.45C= ENSP00000355896.4:p.Val15=
ENST00000366930.8:c.45C= ENSP00000355897.4:p.Val15=
NM_001135599.2:c.45C= NP_001129071.1:p.Val15=
NM_003238.3:c.45C= NP_003229.1:p.Val15=
NM_001135599.3:c.45C= NP_001129071.1:p.Val15=
NM_003238.4:c.45C= NP_003229.1:p.Val15=
NR_138148.1:n.1463C=
NR_138149.1:n.1463C=
NM_003238.5:c.45C= NP_003229.1:p.Val15=
NM_003238.6:c.45C= MANE Select NP_003229.1:p.Val15=
NM_001135599.4:c.45C= NP_001129071.1:p.Val15=
NR_138148.2:n.1411C=
NR_138149.2:n.1411C=