Canonical Allele Identifier: CA1221528075
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345712G= , CM000663.2:g.218345712G= GRCh38
NC_000001.10:g.218519054G= , CM000663.1:g.218519054G= GRCh37
NC_000001.9:g.216585677G= NCBI36
NG_027721.1:g.5379G=
NG_027721.2:g.5379G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-990G= MANE Select ENSP00000355897.4:n.-990G=
NM_001135599.2:c.-990G= NP_001129071.1:n.-990G=
NM_003238.3:c.-990G= NP_003229.1:n.-990G=
NM_001135599.3:c.-990G= NP_001129071.1:n.-990G=
NM_003238.4:c.-990G= NP_003229.1:n.-990G=
NR_138148.1:n.429G=
NR_138149.1:n.429G=
NM_003238.5:c.-990G= NP_003229.1:n.-990G=
NM_003238.6:c.-990G= MANE Select NP_003229.1:n.-990G=
NM_001135599.4:c.-990G= NP_001129071.1:n.-990G=
NR_138148.2:n.377G=
NR_138149.2:n.377G=