Canonical Allele Identifier: CA1148717069

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346679_218346686delinsTTTTTTTT , CM000663.2:g.218346679_218346686delinsTTTTTTTT	GRCh38
NC_000001.10:g.218520021_218520028delinsTTTTTTTT , CM000663.1:g.218520021_218520028delinsTTTTTTTT	GRCh37
NC_000001.9:g.216586644_216586651delinsTTTTTTTT	NCBI36
NG_027721.1:g.6346_6353delinsTTTTTTTT
NG_027721.2:g.6346_6353delinsTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-23_-16delinsTTTTTTTT MANE Select	ENSP00000355897.4:n.-23_-16delinsTTTTTTTT
ENST00000366929.4:c.-23_-16delinsTTTTTTTT	ENSP00000355896.4:n.-23_-16delinsTTTTTTTT
ENST00000366930.8:c.-23_-16delinsTTTTTTTT	ENSP00000355897.4:n.-23_-16delinsTTTTTTTT
NM_001135599.2:c.-23_-16delinsTTTTTTTT	NP_001129071.1:n.-23_-16delinsTTTTTTTT
NM_003238.3:c.-23_-16delinsTTTTTTTT	NP_003229.1:n.-23_-16delinsTTTTTTTT
NM_001135599.3:c.-23_-16delinsTTTTTTTT	NP_001129071.1:n.-23_-16delinsTTTTTTTT
NM_003238.4:c.-23_-16delinsTTTTTTTT	NP_003229.1:n.-23_-16delinsTTTTTTTT
NR_138148.1:n.1396_1403delinsTTTTTTTT
NR_138149.1:n.1396_1403delinsTTTTTTTT
NM_003238.5:c.-23_-16delinsTTTTTTTT	NP_003229.1:n.-23_-16delinsTTTTTTTT
NM_003238.6:c.-23_-16delinsTTTTTTTT MANE Select	NP_003229.1:n.-23_-16delinsTTTTTTTT
NM_001135599.4:c.-23_-16delinsTTTTTTTT	NP_001129071.1:n.-23_-16delinsTTTTTTTT
NR_138148.2:n.1344_1351delinsTTTTTTTT
NR_138149.2:n.1344_1351delinsTTTTTTTT