Canonical Allele Identifier: CA2650532738

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218441556-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441563del , CM000663.2:g.218441563del	GRCh38
NC_000001.10:g.218614905del , CM000663.1:g.218614905del	GRCh37
NC_000001.9:g.216681528del	NCBI36
NG_027721.1:g.101230del
NG_027721.2:g.101230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*201del MANE Select	ENSP00000355897.4:n.*201del
ENST00000366929.4:c.*201del	ENSP00000355896.4:n.*201del
ENST00000366930.8:c.*201del	ENSP00000355897.4:n.*201del
ENST00000479322.1:n.930del
NM_001135599.2:c.*201del	NP_001129071.1:n.*201del
NM_003238.3:c.*201del	NP_003229.1:n.*201del
NM_001135599.3:c.*201del	NP_001129071.1:n.*201del
NM_003238.4:c.*201del	NP_003229.1:n.*201del
NR_138148.1:n.2749del
NR_138149.1:n.2833del
NM_003238.5:c.*201del	NP_003229.1:n.*201del
NM_003238.6:c.*201del MANE Select	NP_003229.1:n.*201del
NM_001135599.4:c.*201del	NP_001129071.1:n.*201del
NR_138148.2:n.2697del
NR_138149.2:n.2781del