Canonical Allele Identifier: CA2747782698

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437514_218437515del , CM000663.2:g.218437514_218437515del	GRCh38
NC_000001.10:g.218610856_218610857del , CM000663.1:g.218610856_218610857del	GRCh37
NC_000001.9:g.216677479_216677480del	NCBI36
NG_027721.1:g.97181_97182del
NG_027721.2:g.97181_97182del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1086+18_1086+19del MANE Select	ENSP00000355897.4:n.1086+18_1086+19del
ENST00000366929.4:c.1170+18_1170+19del	ENSP00000355896.4:n.1170+18_1170+19del
ENST00000366930.8:c.1086+18_1086+19del	ENSP00000355897.4:n.1086+18_1086+19del
ENST00000479322.1:n.570+18_570+19del
NM_001135599.2:c.1170+18_1170+19del	NP_001129071.1:n.1170+18_1170+19del
NM_003238.3:c.1086+18_1086+19del	NP_003229.1:n.1086+18_1086+19del
NM_001135599.3:c.1170+18_1170+19del	NP_001129071.1:n.1170+18_1170+19del
NM_003238.4:c.1086+18_1086+19del	NP_003229.1:n.1086+18_1086+19del
NR_138148.1:n.2389+18_2389+19del
NR_138149.1:n.2473+18_2473+19del
NM_003238.5:c.1086+18_1086+19del	NP_003229.1:n.1086+18_1086+19del
NM_003238.6:c.1086+18_1086+19del MANE Select	NP_003229.1:n.1086+18_1086+19del
NM_001135599.4:c.1170+18_1170+19del	NP_001129071.1:n.1170+18_1170+19del
NR_138148.2:n.2337+18_2337+19del
NR_138149.2:n.2421+18_2421+19del