Canonical Allele Identifier: CA1221528704
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346943A= , CM000663.2:g.218346943A= GRCh38
NC_000001.10:g.218520285A= , CM000663.1:g.218520285A= GRCh37
NC_000001.9:g.216586908A= NCBI36
NG_027721.1:g.6610A=
NG_027721.2:g.6610A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.242A= MANE Select ENSP00000355897.4:p.Lys81=
ENST00000366929.4:c.242A= ENSP00000355896.4:p.Lys81=
ENST00000366930.8:c.242A= ENSP00000355897.4:p.Lys81=
NM_001135599.2:c.242A= NP_001129071.1:p.Lys81=
NM_003238.3:c.242A= NP_003229.1:p.Lys81=
NM_001135599.3:c.242A= NP_001129071.1:p.Lys81=
NM_003238.4:c.242A= NP_003229.1:p.Lys81=
NR_138148.1:n.1660A=
NR_138149.1:n.1660A=
NM_003238.5:c.242A= NP_003229.1:p.Lys81=
NM_003238.6:c.242A= MANE Select NP_003229.1:p.Lys81=
NM_001135599.4:c.242A= NP_001129071.1:p.Lys81=
NR_138148.2:n.1608A=
NR_138149.2:n.1608A=