Canonical Allele Identifier: CA2650531282
Gene: TGFB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218346688_218346690del , CM000663.2:g.218346688_218346690del GRCh38
NC_000001.10:g.218520030_218520032del , CM000663.1:g.218520030_218520032del GRCh37
NC_000001.9:g.216586653_216586655del NCBI36
NG_027721.1:g.6355_6357del
NG_027721.2:g.6355_6357del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-14_-12del MANE Select ENSP00000355897.4:n.-14_-12del
ENST00000366929.4:c.-14_-12del ENSP00000355896.4:n.-14_-12del
ENST00000366930.8:c.-14_-12del ENSP00000355897.4:n.-14_-12del
NM_001135599.2:c.-14_-12del NP_001129071.1:n.-14_-12del
NM_003238.3:c.-14_-12del NP_003229.1:n.-14_-12del
NM_001135599.3:c.-14_-12del NP_001129071.1:n.-14_-12del
NM_003238.4:c.-14_-12del NP_003229.1:n.-14_-12del
NR_138148.1:n.1405_1407del
NR_138149.1:n.1405_1407del
NM_003238.5:c.-14_-12del NP_003229.1:n.-14_-12del
NM_003238.6:c.-14_-12del MANE Select NP_003229.1:n.-14_-12del
NM_001135599.4:c.-14_-12del NP_001129071.1:n.-14_-12del
NR_138148.2:n.1353_1355del
NR_138149.2:n.1353_1355del