Canonical Allele Identifier: CA1221527933
Gene: TGFB2 HGNC NCBI
TGFB2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.218345372_218345373delinsCG , CM000663.2:g.218345372_218345373delinsCG GRCh38
NC_000001.10:g.218518714_218518715delinsCG , CM000663.1:g.218518714_218518715delinsCG GRCh37
NC_000001.9:g.216585337_216585338delinsCG NCBI36
NG_027721.1:g.5039_5040delinsCG
NG_027721.2:g.5039_5040delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366930.9:c.-1330_-1329delinsCG (TGFB2) MANE Select ENSP00000355897.4:n.-1330_-1329delinsCG
NM_001135599.2:c.-1330_-1329delinsCG (TGFB2) NP_001129071.1:n.-1330_-1329delinsCG
NM_003238.3:c.-1330_-1329delinsCG (TGFB2) NP_003229.1:n.-1330_-1329delinsCG
NR_046268.1:n.92_93delinsCG (TGFB2-AS1)
NM_001135599.3:c.-1330_-1329delinsCG (TGFB2) NP_001129071.1:n.-1330_-1329delinsCG
NM_003238.4:c.-1330_-1329delinsCG (TGFB2) NP_003229.1:n.-1330_-1329delinsCG
NR_138148.1:n.89_90delinsCG (TGFB2)
NR_138149.1:n.89_90delinsCG (TGFB2)
NM_003238.5:c.-1330_-1329delinsCG (TGFB2) NP_003229.1:n.-1330_-1329delinsCG
NM_003238.6:c.-1330_-1329delinsCG (TGFB2) MANE Select NP_003229.1:n.-1330_-1329delinsCG
NM_001135599.4:c.-1330_-1329delinsCG (TGFB2) NP_001129071.1:n.-1330_-1329delinsCG
NR_138148.2:n.37_38delinsCG (TGFB2)
NR_138149.2:n.37_38delinsCG (TGFB2)