Canonical Allele Identifier: CA1221528582

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346649_218346650delinsCT , CM000663.2:g.218346649_218346650delinsCT	GRCh38
NC_000001.10:g.218519991_218519992delinsCT , CM000663.1:g.218519991_218519992delinsCT	GRCh37
NC_000001.9:g.216586614_216586615delinsCT	NCBI36
NG_027721.1:g.6316_6317delinsCT
NG_027721.2:g.6316_6317delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-53_-52delinsCT MANE Select	ENSP00000355897.4:n.-53_-52delinsCT
ENST00000366929.4:c.-53_-52delinsCT	ENSP00000355896.4:n.-53_-52delinsCT
ENST00000366930.8:c.-53_-52delinsCT	ENSP00000355897.4:n.-53_-52delinsCT
NM_001135599.2:c.-53_-52delinsCT	NP_001129071.1:n.-53_-52delinsCT
NM_003238.3:c.-53_-52delinsCT	NP_003229.1:n.-53_-52delinsCT
NM_001135599.3:c.-53_-52delinsCT	NP_001129071.1:n.-53_-52delinsCT
NM_003238.4:c.-53_-52delinsCT	NP_003229.1:n.-53_-52delinsCT
NR_138148.1:n.1366_1367delinsCT
NR_138149.1:n.1366_1367delinsCT
NM_003238.5:c.-53_-52delinsCT	NP_003229.1:n.-53_-52delinsCT
NM_003238.6:c.-53_-52delinsCT MANE Select	NP_003229.1:n.-53_-52delinsCT
NM_001135599.4:c.-53_-52delinsCT	NP_001129071.1:n.-53_-52delinsCT
NR_138148.2:n.1314_1315delinsCT
NR_138149.2:n.1314_1315delinsCT