Canonical Allele Identifier: CA2650531292
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346702dup , CM000663.2:g.218346702dup GRCh38
NC_000001.10:g.218520044dup , CM000663.1:g.218520044dup GRCh37
NC_000001.9:g.216586667dup NCBI36
NG_027721.1:g.6369dup
NG_027721.2:g.6369dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.1dup MANE Select ENSP00000355897.4:p.Met1AsnfsTer?
ENST00000366929.4:c.1dup ENSP00000355896.4:p.Met1AsnfsTer?
ENST00000366930.8:c.1dup ENSP00000355897.4:p.Met1AsnfsTer?
NM_001135599.2:c.1dup NP_001129071.1:p.Met1AsnfsTer?
NM_003238.3:c.1dup NP_003229.1:p.Met1AsnfsTer?
NM_001135599.3:c.1dup NP_001129071.1:p.Met1AsnfsTer?
NM_003238.4:c.1dup NP_003229.1:p.Met1AsnfsTer?
NR_138148.1:n.1419dup
NR_138149.1:n.1419dup
NM_003238.5:c.1dup NP_003229.1:p.Met1AsnfsTer?
NM_003238.6:c.1dup MANE Select NP_003229.1:p.Met1AsnfsTer?
NM_001135599.4:c.1dup NP_001129071.1:p.Met1AsnfsTer?
NR_138148.2:n.1367dup
NR_138149.2:n.1367dup