Canonical Allele Identifier: CA322262
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218436036dup , CM000663.2:g.218436036dup GRCh38
NC_000001.10:g.218609378dup , CM000663.1:g.218609378dup GRCh37
NC_000001.9:g.216676001dup NCBI36
NG_027721.1:g.95703dup
NG_027721.2:g.95703dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.821dup MANE Select ENSP00000355897.4:p.Asn274LysfsTer19
ENST00000366929.4:c.905dup ENSP00000355896.4:p.Asn302LysfsTer19
ENST00000366930.8:c.821dup ENSP00000355897.4:p.Asn274LysfsTer19
ENST00000479322.1:n.305dup
NM_001135599.2:c.905dup NP_001129071.1:p.Asn302LysfsTer19
NM_003238.3:c.821dup NP_003229.1:p.Asn274LysfsTer19
NM_001135599.3:c.905dup NP_001129071.1:p.Asn302LysfsTer19
NM_003238.4:c.821dup NP_003229.1:p.Asn274LysfsTer19
NR_138148.1:n.2173-49dup
NR_138149.1:n.2257-49dup
NM_003238.5:c.821dup NP_003229.1:p.Asn274LysfsTer19
NM_003238.6:c.821dup MANE Select NP_003229.1:p.Asn274LysfsTer19
NM_001135599.4:c.905dup NP_001129071.1:p.Asn302LysfsTer19
NR_138148.2:n.2121-49dup
NR_138149.2:n.2205-49dup