Canonical Allele Identifier: CA1221528065
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345688C= , CM000663.2:g.218345688C= GRCh38
NC_000001.10:g.218519030C= , CM000663.1:g.218519030C= GRCh37
NC_000001.9:g.216585653C= NCBI36
NG_027721.1:g.5355C=
NG_027721.2:g.5355C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-1014C= MANE Select ENSP00000355897.4:n.-1014C=
NM_001135599.2:c.-1014C= NP_001129071.1:n.-1014C=
NM_003238.3:c.-1014C= NP_003229.1:n.-1014C=
NM_001135599.3:c.-1014C= NP_001129071.1:n.-1014C=
NM_003238.4:c.-1014C= NP_003229.1:n.-1014C=
NR_138148.1:n.405C=
NR_138149.1:n.405C=
NM_003238.5:c.-1014C= NP_003229.1:n.-1014C=
NM_003238.6:c.-1014C= MANE Select NP_003229.1:n.-1014C=
NM_001135599.4:c.-1014C= NP_001129071.1:n.-1014C=
NR_138148.2:n.353C=
NR_138149.2:n.353C=