Canonical Allele Identifier: CA2747787052
Gene: TGFB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346688dup , CM000663.2:g.218346688dup GRCh38
NC_000001.10:g.218520030dup , CM000663.1:g.218520030dup GRCh37
NC_000001.9:g.216586653dup NCBI36
NG_027721.1:g.6355dup
NG_027721.2:g.6355dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-14dup MANE Select ENSP00000355897.4:n.-14dup
ENST00000366929.4:c.-14dup ENSP00000355896.4:n.-14dup
ENST00000366930.8:c.-14dup ENSP00000355897.4:n.-14dup
NM_001135599.2:c.-14dup NP_001129071.1:n.-14dup
NM_003238.3:c.-14dup NP_003229.1:n.-14dup
NM_001135599.3:c.-14dup NP_001129071.1:n.-14dup
NM_003238.4:c.-14dup NP_003229.1:n.-14dup
NR_138148.1:n.1405dup
NR_138149.1:n.1405dup
NM_003238.5:c.-14dup NP_003229.1:n.-14dup
NM_003238.6:c.-14dup MANE Select NP_003229.1:n.-14dup
NM_001135599.4:c.-14dup NP_001129071.1:n.-14dup
NR_138148.2:n.1353dup
NR_138149.2:n.1353dup